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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
Jul 25, 2014 SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for t... The integrity of the wires inside main electrical chord become compromised from excessive flexing... Class II JK Products & Services, Inc
May 7, 2012 BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For hum... The Beauty Angel was marketed without a 510k. Class II JK Products & Services, Inc
Jul 8, 2005 SUN|DASH RADIUS 252 tanning system; 52 lamps, Ultraviolet Radiation. The d... The firm has tracked a systematic failure in the door cord on the Sun|Dash Radius 252 product lin... Class II JK Products & Services, 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.