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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
Oct 9, 2025 Brand Name: Catalyst+ Product Name: Catalyst, Catalyst+ Model/Catalog Numbe... Due to issues with the system's stereotactic radiosurgery (SRS) treatment cannot be guaranteed fo... Class II C-RAD POSITIONING AB
Apr 22, 2025 Brand Name: Catalyst+ Product Name: C4D software used in conjunction with ... Software issue with scanning equipment that can results in the filed rotation not being applied c... Class II C-RAD POSITIONING AB
Aug 6, 2020 PC Application Software c4D as part of the device Catalyst: SP-002 Software P... PC Application Software c4D not changing Site upon synchronization during the Setup workflow step Class II C-RAD POSITIONING AB

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.