Browse Device Recalls

6 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 6 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 6 FDA device recalls.

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DateProductReasonClassFirm
Apr 27, 2021 The Better-Bladder (BB), part of extracorporeal membrane oxygenation (ECMO) c... The device is used as part of extracorporeal membrane oxygenation (ECMO) cardiopulmonary bypass c... Class II Circulatory Technology Inc.
Sep 22, 2017 Better-Bladder cardiopulmonary bypass blood reservoir; Models: BB14 (individu... The device is used as part of extracorporeal membrane oxygenation (ECMO) cardiopulmonary bypass c... Class II Circulatory Technology Inc
Sep 22, 2017 **Recall Expanded to add these models: Bigger Better-Bladder cardiopulmonary ... The device is used as part of extracorporeal membrane oxygenation (ECMO) cardiopulmonary bypass c... Class II Circulatory Technology Inc
Jul 1, 2016 The Better-Bladder With 14" ID tubing, ITEM BB14, STERILE, Measure pressur... Twisted or wrinkled balloon components which are considered a cosmetic defect by the firm. Class III Circulatory Technology Inc
Jul 1, 2016 The Bigger-Better-Bladder, TM 2 With 3/8"ID tubing, 72" long tubing, ITEM BBB... The seal between the balloon and the housing may leak. Class II Circulatory Technology Inc
Mar 3, 2016 Bigger-Better-Bladder With 3/8" ID tubing, ITEM BBB38 The seal between the balloon and the housing may leak. Class II Circulatory Technology 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.