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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 10, 2019 Luer Lock Set - Catalog # MPC-125, for IV administration sets. Mislabeling - Some unit of sale packages (bags of 100 sets of MPC-125) were found to be incorrect... Class II Molded Products Inc
Jan 20, 2015 Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for ... A customer relayed a complaint of a leaking dialysis tubing connector. Class II Molded Products Inc
Jun 19, 2012 Sterile Access & Return Line Set, 36" Length, Part # UM-872-36. Intended... The recalled product leaks at the connection site. Class II Molded Products Inc

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.