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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
Feb 26, 2020 The CapsoCam Plus (SV-3); Device Common Name: System, Imaging, Gastrointestin... Ingestible video capsule system has capsule with incorrect capture mode which will not record dat... Class II Capso Vision, Inc.
Oct 18, 2019 CapsoCAM Plus, UDI: 00867770000209 Capsule Endoscopy System: a defect present in the capsule window may be stressed through the prod... Class II Capso Vision, Inc.
Jul 3, 2019 CapsoCam Plus *** System, Imaging, Gastrointestinal, Wireless, Capsule, Elect... Possible mis-labeling of the device with incorrect serial number labels which may result in a pat... Class II Capso Vision, 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.