How do I know if my Philips Medical Systems Nederland B.v product is part of a recall?

Compare the lot code, UPC, model number or dates on your product with the official recall notice linked on this page. Our lot/UPC checker searches the official text but is not a guarantee.

What should I do if my Philips Medical Systems Nederland B.v product is recalled?

Follow the instructions in the official notice from the agency (FDA, USDA FSIS, CPSC or NHTSA), such as stopping use, returning or discarding the product, or contacting the company.

Is Philips Medical Systems Nederland B.v recalled?

Philips Medical Systems Nederland B.v recalls - full list & free alerts

Official U.S. agency records list 76 recalls involving Philips Medical Systems Nederland B.v in the last 12 months, most recently on 2026-08-19. Check each official notice for the exact products, lot codes and dates affected.

Check a lot code, UPC or model number

This is not a guarantee; check the official notice.

Recalls (76)

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional fluoroscopic x-ray system.

Medical DevicesFDA (device) · 2026-08-19 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips Azurion Rystem, Model Numbers: 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222,722223, 722224, 722225, 722226, 7222

Medical DevicesFDA (device) · 2026-08-19 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips Azurion, Model Numbers: 722229, 722230, 722231, 722232, 722233, 722234, 722235, and 722236, with Software Version Numbers: R3.0 an

Medical DevicesFDA (device) · 2026-08-19 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips Allura under the following System Descriptions and corresponding model numbers: 1. Allura Xper FD10; Model Numbers: 722003, 722010

Medical DevicesFDA (device) · 2026-08-12 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips Azurion under the following System Descriptions and corresponding model numbers: 1. Azurion 3 M12; Model Numbers: 722063, 722221.

Medical DevicesFDA (device) · 2026-08-12 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional Fluoroscopic X-Ray System.

Medical DevicesFDA (device) · 2026-08-12 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032 for MultiDiagnost Eleva; Model # 708034 for MultiDiagnost E

Medical DevicesFDA (device) · 2026-06-24 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips Allura Xper with the following Model Numbers: Model # 722001 for Allura Xper FD10C; Model # 722002 for Allura Xper FD10F; Model # 72

Medical DevicesFDA (device) · 2026-06-24 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips Azurion 3M12, Model Numbers: 722063, 722221 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Sof

Medical DevicesFDA (device) · 2026-06-10 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips Azurion 3M15, Model Numbers: 722064, 722222 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro So

Medical DevicesFDA (device) · 2026-06-10 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips Azurion 5M12, Model Numbers: 722227 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software k

Medical DevicesFDA (device) · 2026-06-10 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips Azurion 5M20, Model Numbers: 722228 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software k

Medical DevicesFDA (device) · 2026-06-10 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips Azurion 7B12/12, Model Numbers: 722067, 722225 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro

Medical DevicesFDA (device) · 2026-06-10 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips Azurion 7B20/15, Model Numbers: 722068, 722226 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro

Medical DevicesFDA (device) · 2026-06-10 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips Azurion 7M12, Model Numbers: 722078, 722223 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro So

Medical DevicesFDA (device) · 2026-06-10 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips Azurion 7M20, Model Numbers: 722079, 722224 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro So

Medical DevicesFDA (device) · 2026-06-10 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222), Azurion 5 M12 (7222

Medical DevicesFDA (device) · 2026-06-03 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10 OR Table (722022, 722033

Medical DevicesFDA (device) · 2026-06-03 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below product descriptions and corresponding mode

Medical DevicesFDA (device) · 2026-05-27 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12 (722067), Azurion 7 B

Medical DevicesFDA (device) · 2026-05-27 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Allura system; System Code Description (Model Numbers): Allura Xper FD10C (722001), Allura Xper FD10F (722002), Allura Xper FD10 (722003, 72

Medical DevicesFDA (device) · 2026-05-27 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-Nicol (722030), Integris Allura 15 & 12 (

Medical DevicesFDA (device) · 2026-05-27 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips Azurion. System Code Description (Model Number): Azurion 3 M12 (722221, 722229), Azurion 3 M15 (722222, 722230), Azurion 5 (722281),

Medical DevicesFDA (device) · 2026-05-20 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips AneurysmFlow. Model Number: 001015. AneurysmFlow is a software medical device (Interventional Tool) intended to be used in combi

Medical DevicesFDA (device) · 2026-04-22 · Class II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Allura Xper FD10C; System Code: 722001;