{
 "version": "https://jsonfeed.org/version/1.1",
 "title": "RecallRadar – latest U.S. recalls",
 "home_page_url": "https://recallradaralerts.com/",
 "feed_url": "https://recallradaralerts.com/feed.json",
 "description": "Official FDA, USDA FSIS, CPSC and NHTSA recall notices, restated plainly.",
 "language": "en-US",
 "items": [
  {
   "id": "cpsc-27024",
   "url": "https://recallradaralerts.com/r/cpsc-27024.html",
   "external_url": "https://cpsc.gov/Recalls/2027/3M-Company-Recalls-ScotchTM-Thermal-Laminators-Due-to-Risk-of-Serious-Injury-or-Death-from-Fire-Hazard",
   "title": "3M Company Recalls Scotch™ Thermal Laminators Due to Risk of Serious Injury or Death from Fire Hazard",
   "content_text": "CPSC Consumer Products recall: The recalled thermal laminators can overheat, posing a fire hazard.",
   "date_published": "2026-10-15T00:00:00Z",
   "tags": [
    "Consumer Products",
    "CPSC"
   ]
  },
  {
   "id": "cpsc-27025",
   "url": "https://recallradaralerts.com/r/cpsc-27025.html",
   "external_url": "https://cpsc.gov/Recalls/2027/HatsanUSA-Recalls-Blitz-Air-Rifles-Due-to-Risk-of-Serious-Injury-or-Death-from-Projectile-Hazard",
   "title": "HatsanUSA Recalls Blitz Air Rifles Due to Risk of Serious Injury or Death from Projectile Hazard",
   "content_text": "CPSC Consumer Products recall: The recalled air rifles can fire unexpectedly when releasing the bolt before the air rifle is fully cocked, posing a risk of serious injury or death from projectile hazard.",
   "date_published": "2026-10-15T00:00:00Z",
   "tags": [
    "Consumer Products",
    "CPSC"
   ]
  },
  {
   "id": "cpsc-27026",
   "url": "https://recallradaralerts.com/r/cpsc-27026.html",
   "external_url": "https://cpsc.gov/Recalls/2027/Loving-Thyself-Rocks-Recalls-Crystal-Glass-Cups-Due-to-Risk-of-Serious-Injury-from-Ingestion-and-Laceration-Hazards",
   "title": "Loving Thyself Rocks Recalls Crystal Glass Cups Due to Risk of Serious Injury from Ingestion and Laceration Hazards",
   "content_text": "CPSC Consumer Products recall: Glass can break inside the recalled cups while in use, posing a risk of serious injury from ingestion and laceration hazards.",
   "date_published": "2026-10-15T00:00:00Z",
   "tags": [
    "Consumer Products",
    "CPSC"
   ]
  },
  {
   "id": "cpsc-27027",
   "url": "https://recallradaralerts.com/r/cpsc-27027.html",
   "external_url": "https://cpsc.gov/Recalls/2027/Papablic-of-USA-Recalls-Convertible-Bedside-Sleepers-Due-to-Risk-of-Serious-Injury-or-Death-from-Entrapment-Suffocation-and-Fall-Hazards-Violate-Mandatory-Standard-for-Play-Yards",
   "title": "Papablic, of USA Recalls Convertible Bedside Sleepers Due to Risk of Serious Injury or Death from Entrapment, Suffocation and Fall Hazards; Violate Mandatory Standard for Play Yards",
   "content_text": "CPSC Consumer Products recall: The bedside sleepers with play yard extensions violate the mandatory safety standard for play yards because the mattress can become displaced, causing a baby to become entrapped between the sleeping pad and bottom posing a deadly suffocation hazard. In addition, the latching and locking mechanism can fail, causing the product to collapse, posing a risk of serious injury or deadly entrapment and fa",
   "date_published": "2026-10-15T00:00:00Z",
   "tags": [
    "Consumer Products",
    "CPSC"
   ]
  },
  {
   "id": "cpsc-27028",
   "url": "https://recallradaralerts.com/r/cpsc-27028.html",
   "external_url": "https://cpsc.gov/Recalls/2027/Primark-Recalls-101-Dalmatians-Faux-Leather-Childrens-Coin-Purses-Due-to-Phthalate-Levels-and-Risk-of-Ingestion",
   "title": "Primark Recalls 101 Dalmatians Faux Leather Children’s Coin Purses Due to Phthalate Levels and Risk of Ingestion",
   "content_text": "CPSC Consumer Products recall: The coin purses contain higher phthalate concentration levels. Phthalates can be harmful if young children are exposed to sufficient amounts, including through ingestion, and certain phthalates have been associated with adverse health effects, particularly effects on development and the hormone system.",
   "date_published": "2026-10-15T00:00:00Z",
   "tags": [
    "Consumer Products",
    "CPSC"
   ]
  },
  {
   "id": "cpsc-27029",
   "url": "https://recallradaralerts.com/r/cpsc-27029.html",
   "external_url": "https://cpsc.gov/Recalls/2027/usOpal-Recalls-Xalirium-Portable-Bed-Rails-Due-to-Risk-of-Serious-Injury-or-Death-from-Entrapment-and-Asphyxiation-Violate-Mandatory-Standard-for-Adult-Portable-Bed-Rails",
   "title": "usOpal Recalls Xalirium Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails",
   "content_text": "CPSC Consumer Products recall: The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. The bed rails do not meet structural stability or retention strap requirements, posing a fall ha",
   "date_published": "2026-10-15T00:00:00Z",
   "tags": [
    "Consumer Products",
    "CPSC"
   ]
  },
  {
   "id": "nhtsa-26E070000",
   "url": "https://recallradaralerts.com/r/nhtsa-26E070000.html",
   "external_url": "https://www.nhtsa.gov/recalls?nhtsaId=26E070000",
   "title": "Lippert: Electrical System:Wiring:Fuses And Circuit Breakers (9999 LIPPERT SEATING POWER CORD)",
   "content_text": "NHTSA Vehicles & Equipment recall: In the event of a short circuit, inadequate protection increases the risk of a fire.",
   "date_published": "2026-10-09T00:00:00Z",
   "tags": [
    "Vehicles & Equipment",
    "NHTSA"
   ]
  },
  {
   "id": "nhtsa-26V667000",
   "url": "https://recallradaralerts.com/r/nhtsa-26V667000.html",
   "external_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V667000",
   "title": "Grand Design RV, LLC: Equipment:Recreational Vehicle/Trailer (2026 GRAND DESIGN IMAGINE, 2027 GRAND DESIGN IMAGINE)",
   "content_text": "NHTSA Vehicles & Equipment recall: Underrated chains can allow the trailer to detach from the tow vehicle, increasing the risk of a crash.",
   "date_published": "2026-10-09T00:00:00Z",
   "tags": [
    "Vehicles & Equipment",
    "NHTSA"
   ]
  },
  {
   "id": "nhtsa-26V668000",
   "url": "https://recallradaralerts.com/r/nhtsa-26V668000.html",
   "external_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V668000",
   "title": "Grand Design RV, LLC: Equipment:Other:Labels (2027 GRAND DESIGN TRANSCEND)",
   "content_text": "NHTSA Vehicles & Equipment recall: Referencing incorrect information can result in installing the wrong size replacement tires or underinflating the tires, increasing the risk of a crash.",
   "date_published": "2026-10-09T00:00:00Z",
   "tags": [
    "Vehicles & Equipment",
    "NHTSA"
   ]
  },
  {
   "id": "nhtsa-26V671000",
   "url": "https://recallradaralerts.com/r/nhtsa-26V671000.html",
   "external_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V671000",
   "title": "Volvo Car USA, LLC: Seats:Front Assembly:Head Restraint (2025 VOLVO EX30, 2026 VOLVO EX30, 2026 VOLVO EX30CC)",
   "content_text": "NHTSA Vehicles & Equipment recall: A detached head restraint cushion can increase the risk of injury during a crash.",
   "date_published": "2026-10-09T00:00:00Z",
   "tags": [
    "Vehicles & Equipment",
    "NHTSA"
   ]
  },
  {
   "id": "cpsc-27015",
   "url": "https://recallradaralerts.com/r/cpsc-27015.html",
   "external_url": "https://www.cpsc.gov/Recalls/2027/Giant-Bicycle-Recalls-LED-Light-Keys-Included-with-SureLock-Bike-Lock-Sets-Due-to-Risk-of-Serious-Injury-or-Death-from-Battery-Ingestion-Violates-Mandatory-Standard-for-Consumer-Products-with-Button-Cell-Batteries",
   "title": "Giant Bicycle Recalls LED-Light Keys Included with SureLock Bike Lock Sets Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries",
   "content_text": "CPSC Consumer Products recall: The LED-light key that was included with certain SureLock Bicycle Lock sets violates the mandatory safety standard for consumer products with button cell and coin batteries because the button batteries can be accessed easily by children, posing an ingestion hazard.  Additionally, the packaging and product do not have the warnings required under Reese's Law. When button cell or coin batteries are s",
   "date_published": "2026-10-08T00:00:00Z",
   "tags": [
    "Consumer Products",
    "CPSC"
   ]
  },
  {
   "id": "cpsc-27016",
   "url": "https://recallradaralerts.com/r/cpsc-27016.html",
   "external_url": "https://www.cpsc.gov/Recalls/2027/DR-Power-Equipment-Recalls-Pilot-and-Premier-Trimmer-Mowers-Due-to-Risk-of-Serious-Injury-or-Death-from-Fire-and-Burn-Hazards",
   "title": "DR Power Equipment Recalls Pilot and Premier Trimmer Mowers Due to Risk of Serious Injury or Death from Fire and Burn Hazards",
   "content_text": "CPSC Consumer Products recall: Grass and debris can accumulate in the trimmer mowers and ignite, posing a risk of serious injury or death from fire and burn hazards.",
   "date_published": "2026-10-08T00:00:00Z",
   "tags": [
    "Consumer Products",
    "CPSC"
   ]
  },
  {
   "id": "cpsc-27017",
   "url": "https://recallradaralerts.com/r/cpsc-27017.html",
   "external_url": "https://www.cpsc.gov/Recalls/2027/Decathlon-America-Recalls-Van-Rysel-GRVL-AF-Bicycles-Due-to-Risk-of-Serious-Injury-or-Death-from-Crash-Hazard",
   "title": "Decathlon America Recalls Van Rysel GRVL AF Bicycles Due to Risk of Serious Injury or Death from Crash Hazard",
   "content_text": "CPSC Consumer Products recall: The recalled bicycles' front lock nut can loosen during use, causing the front wheel to dislodge or loosen over time, posing a crash hazard.",
   "date_published": "2026-10-08T00:00:00Z",
   "tags": [
    "Consumer Products",
    "CPSC"
   ]
  },
  {
   "id": "cpsc-27018",
   "url": "https://recallradaralerts.com/r/cpsc-27018.html",
   "external_url": "https://cpsc.gov/Recalls/2027/ONTHEWEI-Recalls-Baby-Bath-Seats-Due-to-Risk-of-Serious-Injury-or-Death-to-Children-from-Drowning-Violate-Mandatory-Standard-for-Infant-Bath-Seats",
   "title": "ONTHEWEI Recalls Baby Bath Seats Due to Risk of Serious Injury or Death to Children from Drowning; Violate Mandatory Standard for Infant Bath Seats",
   "content_text": "CPSC Consumer Products recall: The recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.",
   "date_published": "2026-10-08T00:00:00Z",
   "tags": [
    "Consumer Products",
    "CPSC"
   ]
  },
  {
   "id": "cpsc-27019",
   "url": "https://recallradaralerts.com/r/cpsc-27019.html",
   "external_url": "https://www.cpsc.gov/Recalls/2027/Pacearth-Direct-Recalls-PACEARTH-Swing-Seats-Due-to-Risk-of-Serious-Injury-from-Fall-Hazard",
   "title": "Pacearth Direct Recalls PACEARTH Swing Seats Due to Risk of Serious Injury from Fall Hazard",
   "content_text": "CPSC Consumer Products recall: The seats, metal carabiners or quick links, or webbing straps of the recalled swing seats can break during use, posing a risk of serious injury due to fall hazard.",
   "date_published": "2026-10-08T00:00:00Z",
   "tags": [
    "Consumer Products",
    "CPSC"
   ]
  },
  {
   "id": "cpsc-27020",
   "url": "https://recallradaralerts.com/r/cpsc-27020.html",
   "external_url": "https://www.cpsc.gov/Recalls/2027/Romorgniz-Recalls-Six-Drawer-Dressers-Due-to-Risk-of-Serious-Injury-or-Death-from-Tip-Over-and-Entrapment-Hazards-Violate-Mandatory-Standard-for-Clothing-Storage-Units",
   "title": "Romorgniz Recalls Six-Drawer Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units",
   "content_text": "CPSC Consumer Products recall: The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety standards as required by the  STURDY Act.",
   "date_published": "2026-10-08T00:00:00Z",
   "tags": [
    "Consumer Products",
    "CPSC"
   ]
  },
  {
   "id": "cpsc-27021",
   "url": "https://recallradaralerts.com/r/cpsc-27021.html",
   "external_url": "https://www.cpsc.gov/Recalls/2027/Snow-Peak-Recalls-Propane-Fireplace-Inserts-and-Lava-Rocks-Due-to-Risk-of-Serious-Injury-or-Death-from-Burn-and-Fire-Hazards",
   "title": "Snow Peak Recalls Propane Fireplace Inserts and Lava Rocks Due to Risk of Serious Injury or Death from Burn and Fire Hazards",
   "content_text": "CPSC Consumer Products recall: The fireplace's lava rocks can ignite and explode when heated in the propane insert, posing a risk of serious injury or death from burn and fire hazards.",
   "date_published": "2026-10-08T00:00:00Z",
   "tags": [
    "Consumer Products",
    "CPSC"
   ]
  },
  {
   "id": "cpsc-27022",
   "url": "https://recallradaralerts.com/r/cpsc-27022.html",
   "external_url": "https://www.cpsc.gov/Recalls/2027/The-Conqueror-Recalls-Avengers-Medals-Due-to-Risk-of-Serious-Injury-or-Death-from-Magnet-Ingestion-Violate-Mandatory-Standard-for-Magnets",
   "title": "The Conqueror Recalls Avengers Medals Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Magnets",
   "content_text": "CPSC Consumer Products recall: The recalled medals violate the mandatory safety standard for magnets because the high-powered magnets may detach, posing a deadly ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other or other metal objects and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood pois",
   "date_published": "2026-10-08T00:00:00Z",
   "tags": [
    "Consumer Products",
    "CPSC"
   ]
  },
  {
   "id": "nhtsa-26V662000",
   "url": "https://recallradaralerts.com/r/nhtsa-26V662000.html",
   "external_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V662000",
   "title": "Tiffin Motorhomes, Inc.: Fuel System, Diesel:Delivery:Hoses, Lines/Piping, And Fittings (2022 TIFFIN ALLEGRO BUS, 2022 TIFFIN PHAETON, 2023 TIFFIN ALLEGRO BUS…)",
   "content_text": "NHTSA Vehicles & Equipment recall: A fuel leak in the presence of an ignition source increases the risk of a fire. An engine stall increases the risk of a crash.",
   "date_published": "2026-10-08T00:00:00Z",
   "tags": [
    "Vehicles & Equipment",
    "NHTSA"
   ]
  },
  {
   "id": "nhtsa-26V663000",
   "url": "https://recallradaralerts.com/r/nhtsa-26V663000.html",
   "external_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V663000",
   "title": "Honda (American Honda Motor Co.): Tires:Temporary/Emergency Spare Tire (2023 HONDA ACCORD HYBRID, 2023 HONDA CR-V HYBRID, 2024 HONDA ACCORD HYBRID…)",
   "content_text": "NHTSA Vehicles & Equipment recall: A detached bottle cap can become a projectile and strike the user or others nearby, increasing the risk of injury.",
   "date_published": "2026-10-08T00:00:00Z",
   "tags": [
    "Vehicles & Equipment",
    "NHTSA"
   ]
  },
  {
   "id": "nhtsa-26V664000",
   "url": "https://recallradaralerts.com/r/nhtsa-26V664000.html",
   "external_url": "https://www.nhtsa.gov/recalls?nhtsaId=26V664000",
   "title": "Hyundai Motor America: Seats:Front Assembly:Power Adjust (2015 HYUNDAI GENESIS, 2016 HYUNDAI GENESIS, 2017 GENESIS G80…)",
   "content_text": "NHTSA Vehicles & Equipment recall: A fire increases the risk of injury.",
   "date_published": "2026-10-08T00:00:00Z",
   "tags": [
    "Vehicles & Equipment",
    "NHTSA"
   ]
  },
  {
   "id": "fda-device-Z-0003-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0003-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 30\" X 4\" 1-LINE (CS 18) WHITE  Model/Catalog Number: 553322  Software Ver",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0004-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0004-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 30\" X 4\" 2-LINE (CS 18) WHITE  Model/Catalog Number: 553323  Software Ver",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0005-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0005-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 8\" X 2.5\" 2-LINE (CS 10)  Model/Catalog Number: 564001  Software Version:",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0006-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0006-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 12\" X 3.5\" 2-LINE (CS 10) PLUM  Model/Catalog Number: 564003  Software Ve",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0007-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0007-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 15\" X 4\" 2-LINE (CS 10) GRAY  Model/Catalog Number: 564005  Software Vers",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0008-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0008-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 18\" X 4\" 1-LINE (CS 10) RED  Model/Catalog Number: 564006  Software Versi",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0009-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0009-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 18\" X 4\" 2-LINE (CS 10) RED  Model/Catalog Number: 564007  Software Versi",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0010-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0010-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 24\" X 4\" 1-LINE (CS 10) YELLOW  Model/Catalog Number: 564008  Software Ve",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0011-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0011-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 24\" X 4\" 2-LINE (CS 10) YELLOW  Model/Catalog Number: 564009  Software Ve",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0012-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0012-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 30\" X 4\" 1-LINE (CS 10) WHITE  Model/Catalog Number: 564010  Software Ver",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0013-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0013-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 30\" X 4\" 2-LINE (CS 10) WHITE  Model/Catalog Number: 564011  Software Ver",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0014-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0014-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 34\" X 4\" 1-LINE (CS 10) BLUE  Model/Catalog Number: 564012  Software Vers",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0015-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0015-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 34\" X 4\" 2-LINE (CS 10) BLUE  Model/Catalog Number: 564013  Software Vers",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0016-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0016-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 44\" X 4\" 1-LINE (CS 10) GREEN  Model/Catalog Number: 564014  Software Ver",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0017-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0017-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 44\" X 4\" 2-LINE (CS 10) GREEN  Model/Catalog Number: 564015  Software Ver",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0018-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0018-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 20\" X 6\" 1-LINE (CS 10) NAVY BLUE  Model/Catalog Number: 564017  Software",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0019-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0019-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 26\" X 6\" 1-LINE (CS 10) ORANGE  Model/Catalog Number: 564019  Software Ve",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0020-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0020-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 38\" X 4\" 1-LINE (CS 10)  Model/Catalog Number: 564044  Software Version: ",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0021-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0021-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 8\" X 2.5\" 1-LINE (CS 12) LIGHT BLUE  Model/Catalog Number: A70107000  Sof",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0022-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0022-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 8\" X 2.5\" 2-LINE (CS 12) LIGHT BLUE  Model/Catalog Number: A70107001  Sof",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0023-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0023-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 12\" X 3.5\" 1-LINE (CS 12) PLUM  Model/Catalog Number: A70107002  Software",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0024-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0024-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 12\" X 3.5\" 2-LINE (CS 12) PLUM  Model/Catalog Number: A70107003  Software",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0025-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0025-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name: DISPOSABLE TOURNIQUET CUFF, 15\" X 4\" 1-LINE (CS 12) GRAY  Model/Catalog Number: A70107004  Software V",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0026-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0026-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name:DISPOSABLE TOURNIQUET CUFF, 15\" X 4\" 2-LINE (CS 12) GRAY  Model/Catalog Number: A70107005  Software Ve",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0027-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0027-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name:DISPOSABLE TOURNIQUET CUFF, 18\" X 4\" 1-LINE (CS 18) RED  Model/Catalog Number: A70107006  Software Ver",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0028-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0028-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name:DISPOSABLE TOURNIQUET CUFF, 18\" X 4\" 2-LINE (CS 18) RED  Model/Catalog Number: A70107007  Software Ver",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0029-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0029-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name:DISPOSABLE TOURNIQUET CUFF, 24\" X 4\" 1-LINE (CS 18) YELLOW  Model/Catalog Number: A70107008  Software ",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0030-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0030-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name:DISPOSABLE TOURNIQUET CUFF, 24\" X 4\" 2-LINE (CS 18) YELLOW  Model/Catalog Number: A70107009  Software ",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0031-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0031-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name:DISPOSABLE TOURNIQUET CUFF, 34\" X 4\" 1-LINE (CS 18) BLUE  Model/Catalog Number: A70107010  Software Ve",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0032-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0032-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name:DISPOSABLE TOURNIQUET CUFF, 34\" X 4\" 2-LINE (CS 18) BLUE  Model/Catalog Number: A70107011  Software Ve",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0033-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0033-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name:DISPOSABLE TOURNIQUET CUFF, 44\" X 4\" 1-LINE (CS 12) GREEN  Model/Catalog Number: A70107012  Software V",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0034-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0034-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name:DISPOSABLE TOURNIQUET CUFF, 44\" X 4\" 2-LINE (CS 12) GREEN  Model/Catalog Number: A70107013  Software V",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0035-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0035-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name:DISPOSABLE BB TOURNQUET CUFF, 20\" X 6\" DUAL BLADDER 1-LINE (CS 12) NAVY BLUE  Model/Catalog Number: A7",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0036-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0036-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name:DISPOSABLE BB TOURNQUET CUFF, 26\" X 6\" DUAL BLADDER, 1-LINE (CS 12) ORANGE  Model/Catalog Number: A701",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0037-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0037-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: Expressaire  Product Name:DISPOSABLE BB TOURNQUET CUFF, 26\" X 6\" DUAL BLADDER, 2-LINE (CS 12) ORANGE    Model/Catalog Number: A7",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0038-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0038-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: ASP Global  Product Name:DISPOSABLE TOURNIQUET CUFF, 12\" X 3.5\" 2-Line, Plum  Model/Catalog Number: ASP-564003  Software Version",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0039-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0039-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: ASP Global  Product Name:DISPOSABLE TOURNIQUET CUFF, 18\" X 4\" 1-Line, Red  Model/Catalog Number: ASP-564006  Software Version: N",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0040-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0040-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: ASP Global  Product Name:DISPOSABLE TOURNIQUET CUFF, 18\" X 4\" 2-Line, Red  Model/Catalog Number: ASP-564007  Software Version: N",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0041-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0041-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: ASP Global  Product Name:DISPOSABLE TOURNIQUET CUFF, 24\" X 4\" 1-Line, Yellow  Model/Catalog Number: ASP-564008  Software Version",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0042-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0042-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: ASP Global  Product Name:DISPOSABLE TOURNIQUET CUFF, 24\" X 4\" 2-Line, Yellow  Model/Catalog Number: ASP-564009  Software Version",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0043-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0043-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: ASP Global  Product Name:DISPOSABLE TOURNIQUET CUFF, 30\" X 4\" 1-Line, White  Model/Catalog Number: ASP-564010  Software Version:",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0044-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0044-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: ASP Global  Product Name:DISPOSABLE TOURNIQUET CUFF, 30\" X 4\" 2-Line, White  Model/Catalog Number: ASP-564011  Software Version:",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0045-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0045-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: ASP Global  Product Name:DISPOSABLE TOURNIQUET CUFF, 34\" X 4\" 1-Line, Blue    Model/Catalog Number: ASP-564012  Software Version",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0046-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0046-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: ASP Global  Product Name:DISPOSABLE TOURNIQUET CUFF, 34\" X 4\" 2-Line, Blue  Model/Catalog Number: ASP-564013  Software Version: ",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0047-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0047-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: ASP Global  Product Name:DISPOSABLE TOURNIQUET CUFF, 44\" X 4\" 1-Line, Green  Model/Catalog Number: ASP-564014  Software Version:",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0048-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0048-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: ASP Global  Product Name:DISPOSABLE TOURNIQUET CUFF, 44\" X 4\" 2-Line, Green    Model/Catalog Number: ASP-564015  Software Versio",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0049-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0049-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:DISPOSABLE TOURNIQUET CUFF 20\" DUAL BLADDER, 1 LINE (10)  Model/Catalog Number: DB-7018-01Q  Software Version:",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0050-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0050-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:DISPOSABLE TOURNIQUET CUFF 20\" DUAL BLADDER, 2 LINE (10)  Model/Catalog Number: DB-7020-02Q  Software Version:",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0051-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0051-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:SINGLE USE TOURNIQUET CUFF 26\" DUAL BLADDER, 2 LINE (10)  Model/Catalog Number: DB-7024-02Q  Software Version:",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0052-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0052-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:SINGLE USE TOURNIQUET CUFF 18\" 1 LINE (10)  Model/Catalog Number: DT-7018-01Q  Software Version: Not Applicabl",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0053-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0053-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:SINGLE USE TOURNIQUET CUFF 24\" 1 LINE (10)  Model/Catalog Number: DT-7024-01Q  Software Version: Not Applicabl",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0054-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0054-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:SINGLE USE TOURNIQUET CUFF 24\" 2 LINE (10)  Model/Catalog Number: DT-7024-02Q  Software Version: Not Applicabl",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0055-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0055-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:SINGLE USE TOURNIQUET CUFF 30\" 1 LINE (10)  Model/Catalog Number: DT-7030-01Q  Software Version: Not Applicabl",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0056-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0056-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:SINGLE USE TOURNIQUET CUFF 30\" 2 LINE (10)  Model/Catalog Number: DT-7030-02Q  Software Version: Not Applicabl",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0057-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0057-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:SINGLE USE TOURNIQUET CUFF 34\" 1 LINE (10)  Model/Catalog Number: DT-7034-01Q  Software Version: Not Applicabl",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0058-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0058-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:SINGLE USE TOURNIQUET CUFF 34\" 2 LINE (10)  Model/Catalog Number: DT-7034-02Q  Software Version: Not Applicabl",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0059-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0059-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:SINGLE USE TOURNIQUET CUFF 44\" 1 LINE (10)  Model/Catalog Number: DT-7044-01Q  Software Version: Not Applicabl",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0060-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0060-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:SINGLE USE TOURNIQUET CUFF 44\" 2 LINE (10)  Model/Catalog Number: DT-7044-02Q  Software Version: Not Applicabl",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0061-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0061-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:SINGLE USE TOURNIQUET CUFF 8\" 2 LINE (10)  Model/Catalog Number: DT-7108-02Q  Software Version: Not Applicable",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0062-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0062-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:SINGLE USE TOURNIQUET CUFF 12\" 1 LINE (10)  Model/Catalog Number: DT-7112-01Q  Software Version: Not Applicabl",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0063-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0063-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:SINGLE USE TOURNIQUET CUFF 12\" 2 LINE (10)  Model/Catalog Number: DT-7112-02Q  Software Version: Not Applicabl",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0064-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0064-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:SINGLE USE TOURNIQUET CUFF 15\" 1 LINE (10)  Model/Catalog Number: DT-7115-01Q  Software Version: Not Applicabl",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0065-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0065-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:SINGLE USE TOURNIQUET CUFF 15\" 2 LINE (10)  Model/Catalog Number: DT-7115-02Q    Software Version: Not Applica",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0066-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0066-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99676",
   "title": "ASP Global, LLC.: Brand Name: MPR  Product Name:DISPOSABLE TOURNIQUET CUFF 18\" 2 LINE (10)  Model/Catalog Number: DT-7218-02Q    Software Version: Not Applica",
   "content_text": "FDA (device) Medical Devices recall: Due to incorrect expiration date on product manufactured between September 2016 to March 2023.  Products are labeled with a 10 year shelf life.  The correct validated shelf life is 5 years.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0067-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0067-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99699",
   "title": "Custom Interventional Pain Management, LLC: Brand Name: Ferndale Laboratories; Medline; Custom Interventional Pain Management CIPM  Product Name: Mastisol Skin Adhesive  Model/Catalog ",
   "content_text": "FDA (device) Medical Devices recall: Due to manufacturing issues with the liquid skin adhesive containing in surgical convenience trays/kits.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-0068-2027",
   "url": "https://recallradaralerts.com/r/fda-device-Z-0068-2027.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99585",
   "title": "Illumina, Inc.: NovaSeq 6000Dx including DRAGEN Server,  Catalog Number: 20068232;   Illumina DRAGEN Server for NextSeq 550Dx, Catalog Number: 20086130",
   "content_text": "FDA (device) Medical Devices recall: Retrospectively reported correction for an instrument intended for targeted sequencing of DNA libraries from human genomic DNA used with in vitro diagnostic assays has a server with a security vulnerability.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-3155-2026",
   "url": "https://recallradaralerts.com/r/fda-device-Z-3155-2026.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99865",
   "title": "Philips North America Llc: Philips Medical Systems  Technologies Ltd. Spectral CT 7500, Software V5.2.x, Product Code 728333",
   "content_text": "FDA (device) Medical Devices recall: The Bolus tracking scan application may crash with a system error message. Bolus Tracker shots may continue to occur even if the contrast threshold is reached. This may result in the patient receiving additional radiation.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-3227-2026",
   "url": "https://recallradaralerts.com/r/fda-device-Z-3227-2026.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99827",
   "title": "Medline Industries, LP: Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories, Hand Pendants:    MDR510094\tPENDANT F/ MDR107002E   MDR520094\tPENDANT",
   "content_text": "FDA (device) Medical Devices recall: Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially leading to smoking, sparking, melting, burning, or fire. Additional products added to 11/26/2025 recall.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-3228-2026",
   "url": "https://recallradaralerts.com/r/fda-device-Z-3228-2026.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99827",
   "title": "Medline Industries, LP: Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories    MDR107000P\tBED, MANUAL, MEDLITE",
   "content_text": "FDA (device) Medical Devices recall: Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially leading to smoking, sparking, melting, burning, or fire. Additional products added to 11/26/2025 recall.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-3252-2026",
   "url": "https://recallradaralerts.com/r/fda-device-Z-3252-2026.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99787",
   "title": "Draeger, Inc.: VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310    Disposable breathing circuit for use with a resuscitation module.",
   "content_text": "FDA (device) Medical Devices recall: Potential cracks in the hose, which could lead to leakage or the hose falling off.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-3270-2026",
   "url": "https://recallradaralerts.com/r/fda-device-Z-3270-2026.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=98483",
   "title": "HeartSine Technologies Ltd: HeartSine samaritan PAD (Public Access Defibrillator);   HeartSine SAM 350P   350P US Device, US English - 2 Min CPR   UDI-DI codes: 0506016",
   "content_text": "FDA (device) Medical Devices recall: Products were distributed without the required Maintenance Supplement, which describes an extra check every 3 months in addition to the monthly check.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-3271-2026",
   "url": "https://recallradaralerts.com/r/fda-device-Z-3271-2026.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99409",
   "title": "Alere San Diego, Inc.: McKesson CONSULT hCG Urine Cassette, Model/ Part: FHC-A102/5001;  Alere hCG Cassette (20 mIU/mL) in Urine, Model/ Part: FHC-A102/92210;  Fis",
   "content_text": "FDA (device) Medical Devices recall: hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-3272-2026",
   "url": "https://recallradaralerts.com/r/fda-device-Z-3272-2026.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99409",
   "title": "Alere San Diego, Inc.: Fisher Scientific Sure-Vue Serum/Urine hCG, Model/ Part: FHC-202/23900529, FHC-202/23900528;    Beckman Coulter Inc's ICON 25 hCG, Model/ Pa",
   "content_text": "FDA (device) Medical Devices recall: hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-3273-2026",
   "url": "https://recallradaralerts.com/r/fda-device-Z-3273-2026.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99409",
   "title": "Alere San Diego, Inc.: Fisher Scientific Sure-Vue Urine hCG Strip, Model/ Part: FHC-101/23900527;  McKesson CONSULT hCG Urine Test Dipstick CLIA Waived, Model/ Par",
   "content_text": "FDA (device) Medical Devices recall: hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-3274-2026",
   "url": "https://recallradaralerts.com/r/fda-device-Z-3274-2026.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99409",
   "title": "Alere San Diego, Inc.: Fisher Scientific Sure-Vue Urine hCG, Model/ Part: FHC-102/23900526;  Henry Schein, Inc. One Step + Urine Cassette Test, Model/ Part: FHC-10",
   "content_text": "FDA (device) Medical Devices recall: hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-3275-2026",
   "url": "https://recallradaralerts.com/r/fda-device-Z-3275-2026.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99590",
   "title": "Bard Peripheral Vascular Inc: EnCor EnCompass Breast Biopsy and Tissue Removal System Console (model number: ENCPCONSOLE) and Driver (model number: ENCPDRIVER) with softw",
   "content_text": "FDA (device) Medical Devices recall: Breast biopsy and tissue removal system may experience the following errors: 1) Probe calibration and /or handheld driver failure (code HH01-00020009) , 2)  Pressure sensor (code E01-0054000E), which prompts the user to restart and re-calibrate; errors may lead to interruption or prolongation of the biopsy procedure, or the need for additional tissue sampling or repeat biopsy.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-3276-2026",
   "url": "https://recallradaralerts.com/r/fda-device-Z-3276-2026.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99730",
   "title": "Volcano Corp: Philips IntraSight Plus  REF: 797423 and 797417  100-120v-220-240v,50/60hZ, 1000 VA",
   "content_text": "FDA (device) Medical Devices recall: Software system  may associate image data from one patient with another patient's record, potentially resulting in incorrect diagnosis or treatment.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-3277-2026",
   "url": "https://recallradaralerts.com/r/fda-device-Z-3277-2026.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99731",
   "title": "Shanghai United Imaging Healthcare Co., Ltd.: Computed Tomography X-ray System, Model: uCT 530 with software",
   "content_text": "FDA (device) Medical Devices recall: Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  },
  {
   "id": "fda-device-Z-3278-2026",
   "url": "https://recallradaralerts.com/r/fda-device-Z-3278-2026.html",
   "external_url": "https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99731",
   "title": "Shanghai United Imaging Healthcare Co., Ltd.: Computed Tomography X-ray System, Model: uCT 550 with software",
   "content_text": "FDA (device) Medical Devices recall: Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.",
   "date_published": "2026-10-07T00:00:00Z",
   "tags": [
    "Medical Devices",
    "FDA (device)"
   ]
  }
 ]
}