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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
Aug 7, 2015 IBC Aortic Punch Catalog Numbers APM40, APL48A, APM44A, APL40A, APM40A, CVAPL... It was discovered that the heat seal placed onto sterile pouches may not meet strength acceptance... Class II International Biophysics Corp.
Aug 7, 2015 IBC Suction Wand Catalog Number 1990S Product Usage: The IBC Suction Wan... It was discovered that the heat seal placed onto sterile pouches may not meet strength acceptance... Class II International Biophysics Corp.
Aug 7, 2015 IBC Vascular Loop Catalog Number CH111, CH112, CH113, CH114, CH115, CH116, CH... It was discovered that the heat seal placed onto sterile pouches may not meet strength acceptance... Class II International Biophysics Corp.

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.