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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
Jun 5, 2025 Brand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog... Due to manufacturing error, Intraosseous device built-in stabilizer may not be released properly ... Class II Waismed Ltd.
Jun 5, 2025 Brand Name: NIO+ Product Name: NIO Intraosseous Device Adult Model/Catalog ... Due to manufacturing error, Intraosseous device built-in stabilizer may not be released properly ... Class II Waismed Ltd.
Aug 18, 2016 NIO-A / NIO-P is an instant IO access device comprises housing with spring lo... WaisMed received a report in which during the operation of the NIO-A, the needle was not released... Class II Waismed Ltd

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.