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Browse Device Recalls

162 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 162 FDA medical device recall enforcement actions. Each entry includes the device description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.

Medical Device Recalls

Browse 162 FDA device recalls.

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DateProductReasonClassFirm
Jul 19, 2023 Azurion A foot switch pedal may get stuck in the active position when the user releases the pedal, resul... Class II Philips Medical Systems Nederland B.V.
Jul 19, 2023 Allura Xper series A foot switch pedal may get stuck in the active position when the user releases the pedal, resul... Class II Philips Medical Systems Nederland B.V.
Jun 30, 2023 Wireless Foot Switch distributed with Philips Allura Xper and Azurion Interve... Loss of availability of the wireless foot switch during procedures. Class II PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Jun 12, 2023 Allura Xper FD10 and FD20. X-ray Imaging System. The bolts supporting the FlexMove Carriage may become loose and/or break, and cracks may appear i... Class II PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Jun 12, 2023 Azurion 7 M20. X-ray Image guided Therapy System. The bolts supporting the FlexMove Carriage may become loose and/or break, and cracks may appear i... Class II PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Mar 21, 2023 Philips Azurion System with software versions: R2.2.O, R2.2.1, R2.2.3, R2.2.... Potential Loss of X-ray-When the full disk capacity is reached, X-Ray functionality will cease to... Class II PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Feb 20, 2023 2D Perfusion, release R1.0.x, R1.1.x, R1.2, and R1.2.1 There are technical issues related to signal generation and processing, which can lead to inaccur... Class II PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Feb 20, 2023 SmartPerfusion, release R1.0, R1.1, R1.1.1, R1.1.5, R1.1.5.1 and R1.1.6 There are technical issues related to signal generation and processing, which can lead to inaccur... Class II PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Dec 2, 2021 Zenition 70, Model #718133 Firm discovered that the wireless foot switch can suddenly stop responding due to a firmware issu... Class II PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Dec 2, 2021 Veradius Unity, Model #718132 Firm discovered that the wireless foot switch can suddenly stop responding due to a firmware issu... Class II PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Dec 2, 2021 Zenition 50, Model #718096 Firm discovered that the wireless foot switch can suddenly stop responding due to a firmware issu... Class II PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
May 26, 2021 Azurion systems with software release R1.x In the Azurion system, the user can add a new study to a patient by selecting the option Add St... Class II PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Frequently Asked Questions

When a device safety issue is identified, the manufacturer or FDA initiates a recall. The FDA publishes an enforcement report detailing the device, the reason for the recall, and distribution. Healthcare facilities and providers are notified to check their inventory and take corrective action.

All types — from simple devices like blood glucose test strips and surgical gloves to complex devices like pacemakers, defibrillators, insulin pumps, hip implants, and ventilators. Software-driven devices are increasingly common in recalls due to bugs and cybersecurity vulnerabilities.

Use the search and filter tools on this page. Each recall entry includes the device description, model numbers, and distribution details so you can determine if your device is affected. Contact your healthcare provider if you find a match.