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Browse Device Recalls

9 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 9 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 9 FDA device recalls.

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DateProductReasonClassFirm
Feb 21, 2024 Thermalon Heating Pad, Item Number 24002 Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessiv... Class II Bruder Healthcare Company, LLC
Feb 21, 2024 MediBeads King Pad, Item Numbers: 34120, 34120PM, 34125R Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessiv... Class II Bruder Healthcare Company, LLC
Feb 21, 2024 Thermalon Eye Compress, Item Number 2434 Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessiv... Class II Bruder Healthcare Company, LLC
Feb 21, 2024 MediBeads Neck Wrap, Item Number 34320 Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessiv... Class II Bruder Healthcare Company, LLC
Feb 21, 2024 Thermalon Neck Wrap, Item Number 24322 Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessiv... Class II Bruder Healthcare Company, LLC
Feb 21, 2024 Thermalon Sinus Compress, Item Number 24332 Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessiv... Class II Bruder Healthcare Company, LLC
Feb 21, 2024 Thermalon Back Wrap, Item Number 24312 Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessiv... Class II Bruder Healthcare Company, LLC
Feb 21, 2024 Thermalon Sinus Compress (French), Item Number 24332F Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessiv... Class II Bruder Healthcare Company, LLC
Feb 21, 2024 Thermalon Stye Compress, Item Number 24352 Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessiv... Class II Bruder Healthcare Company, LLC

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.