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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
Dec 10, 2018 Aperio CS2 CE IVD scanner instrument, scanner part #23CS100CE. The incorrect sensor was used in the assembly of the camera in the scanner instrument which can p... Class II Leica Biosystems Imaging, Inc.
Feb 7, 2014 HER2 Image Analysis Manual Read of HER2 Digital Slides ER/PR Image Analysis... In an abundance of caution, Aperio (now known as Lecia Biosystems) is providing additional inform... Class II Leica Biosystems Imaging, 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.