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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
Jul 27, 2020 Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Product Usage: It is ... Sample leaking from the sleeve covering the needle inside the cannula Class II C.A. Greiner & Sohne Gesellschaftmbh
Apr 3, 2020 VACUETTE Blood Transfer Unit. Lot no. A19024NX. Expiration date: 2022-02-07 -... While transferring blood the needle may dislodged and remain in the tube stopper which may cause ... Class II C.A. Greiner & Sohne Gesellschaftmbh

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.