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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
Jan 19, 2016 Convenience Kits from Centurion that contain an In-Vision- Plus Needleless I... Convenience Kits contain an In-Vision-Plus Needleless IV Connector, code RYM5001 that is being re... Class II Centurion Medical Products Corporation
Jan 5, 2016 InVision-Plus and InVision-Plus Junior Needleless IV Connector, Disposable, S... Potential for the female luer component of the InVision-Plus IV connector to crack during use. Class II Rymed Technologies, LLC
Jan 5, 2016 InVision-Plus CS Needleless IV Connector, Catalog Number RYM-7001. Disposabl... Potential for the female luer component of the InVision-Plus IV connector to crack during use. Class II Rymed Technologies, LLC

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.