⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

Stryker recalls - full list & free alerts

11 official U.S. recalls involving Stryker in the last 12 months, most recently on 2026-08-12.

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Full list (11)

Stryker Corporation: STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600
Medical DevicesFDA (device) · 2026-08-12 · Class II
Stryker Corporation: STRYKER AHTO TUBE SET WITH TIP PACKAGING, Catalog Number 0250070620
Medical DevicesFDA (device) · 2026-08-12 · Class II
Stryker Corporation: STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING, Catalog Number 0250070640
Medical DevicesFDA (device) · 2026-08-12 · Class II
Stryker Corporation: STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530
Medical DevicesFDA (device) · 2026-08-12 · Class II
Stryker Corporation: STRYKER PKG., STRYKEFLOW SUCTION/IRRIGATOR PS, Catalog Number 0250070540
Medical DevicesFDA (device) · 2026-08-12 · Class II
Stryker Corporation: Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
Medical DevicesFDA (device) · 2026-06-10 · Class II
Stryker Corporation: Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube Sets are intended to be used with the Fl
Medical DevicesFDA (device) · 2026-05-20 · Class II
Stryker Corporation: MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN): 00850024195028 MS-00009
Medical DevicesFDA (device) · 2026-02-25 · Class II
Stryker Corporation: NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP; NN-8001 15x 13 MHP; NN-8002 15x 25 MHP - MINOP; NN-8003
Medical DevicesFDA (device) · 2025-12-03 · Class II
Stryker Corporation: NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination Sleeve/Fiber; Product No. NN-1001 13g Illumination Sleeve/Fiber
Medical DevicesFDA (device) · 2025-12-03 · Class II
Stryker Corporation: NICO BrainPath; Product Number/Product Name NN-8024 BrainPath Shephard's Hook - Greenberg; NN-8025 BrainPath Shephard's Hook - Sugita
Medical DevicesFDA (device) · 2025-12-03 · Class II