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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
Jan 29, 2014 Gelzone Shoulder Sleeve, Catalog Number SLV634, Lot Number 852766. Product... Implantech initiated the voluntary recall of Gelzone Shoulder Sleever, SLV-634, Lot Number 852766... Class II Implantech Associates Inc
Aug 30, 2013 Device Name: Terino Square Chin-Style II-Medium; Catalog Number: TSCII-M. ... Implantech initiated a voluntary recall of certain lots of Terino Square Chin-Style II-Medicum (L... Class II Implantech Associates 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.