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Browse Device Recalls

2 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 2 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 2 FDA device recalls.

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DateProductReasonClassFirm
Dec 5, 2013 Symmetry and CODMAN brands, QUAD-LOCK Sterilization Container. Sterilization ... The Quad-Lock Sterilization Container System may not maintain an effective sterile barrier. Class II Symmetry Medical/SSI
Apr 10, 2013 Codman(R) Collins Radioparent Sternal Blade Nylon,4 3/4" (121 mm) long, 3" (... There is a possibility that the Collins Radioparent Sternal Blades Nylon may break during use. Class II Symmetry Medical/SSI

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.