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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
Dec 5, 2022 Turbett Surgical Container, TS1200: Indicated for enclosing other medical dev... Pod may have weld failures breaching the sterile barrier and result in the use of unsterile instr... Class II Turbett Surgical, Inc.
Dec 5, 2022 Turbett Surgical Container, TS1000: Indicated for enclosing other medical dev... Pod may have weld failures breaching the sterile barrier and result in the use of unsterile instr... Class II Turbett Surgical, Inc.
Apr 14, 2022 Turbett Surgical Container, TS1500 Devices were subject to unapproved rework processes. Class II Turbett Surgical, 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.