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

76 official U.S. recalls involving Philips Medical Systems Nederland B.v in the last 12 months, most recently on 2026-08-19.

Check a lot code or UPC for Philips Medical Systems Nederland B.v · Recall guides

Get alerts for Philips Medical Systems Nederland B.v

Full list (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;