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Browse Device Recalls

5 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 5 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 5 FDA device recalls.

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DateProductReasonClassFirm
Oct 6, 2023 D-Clip Standard/Mini Applier, 190mm bayonet, jaw rigid, double action. Customer complaint received that reported the applier failed during surgery. The applier did not ... Class II Peter Lazic Gmbh
Oct 6, 2023 D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action. Customer complaint received that reported the applier failed during surgery. The applier did not ... Class II Peter Lazic Gmbh
Oct 6, 2023 D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action. Customer complaint received that reported the applier failed during surgery. The applier did not ... Class II Peter Lazic Gmbh
Jul 14, 2023 L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile Wrong product coloring. The paddle clips should be blank, but they are colored blue. Class II Peter Lazic Gmbh
Jul 14, 2023 L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Sterile Wrong product coloring. The paddle clips should be blank, but they are colored blue. Class II Peter Lazic Gmbh

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.