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Browse Device Recalls

3 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 3 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 3 FDA device recalls.

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DateProductReasonClassFirm
Mar 24, 2021 Drop Arm Versamode" The front casters on the 6810A Lumex Drop Arm Versamode are incorrect. Class II Gf Health Products
Sep 30, 2016 Lumex, Patriot Full Electric Homecare Bed, & Patriot LX Full Electric Homecar... GF Health Products, Inc., in conjunction with OKIN America, has initiated a voluntary field corre... Class II GF Health Products, Inc
Jul 21, 2014 Zenith Slide W-I-D-E Long Term Care Bed, Model(s) APS98674, APS9867406, APS98... The bed head deck may fail to elevate as expected during normal operation. When the non-operatio... Class II GF Health Products, Inc./d.b.a.Basic American M...

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.