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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
Mar 11, 2021 HydraVision Digital Imaging System Product ID/Reorder Number: 705559 (65KW) Failure to comply with the performance standard for fluoroscopy systems. Per 21 CFR 1020.32(k)(6)... Class II LIEBEL-FLARSHEIM COMPANY LLC
Feb 27, 2017 Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim... Software issue. The difference between the display and dosimeter readings In the Child/Pediatric... Class II LIEBEL-FLARSHEIM COMPANY LLC
Feb 27, 2017 Liebel-Flarsheim Direct Digital Imaging System (DDIS) Liebel-Flarsheim ur... Software issue. The difference between the display and dosimeter readings In the Child/Pediatric... Class II LIEBEL-FLARSHEIM 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.