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Browse Device Recalls

11 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 11 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 11 FDA device recalls.

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DateProductReasonClassFirm
Oct 1, 2025 DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 71... Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2... Class II Philips Medical Systems DMC GmbH
Oct 1, 2025 CombiDiagnost R90; Model Number: 709031; Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2... Class II Philips Medical Systems DMC GmbH
Oct 1, 2025 ProxiDiagnost N90; Model Number: 706110; Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2... Class II Philips Medical Systems DMC GmbH
Oct 1, 2025 Precision CRF; Model Number: 706400; Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2... Class II Philips Medical Systems DMC GmbH
Oct 1, 2025 DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Num... Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2... Class II Philips Medical Systems DMC GmbH
Oct 1, 2025 Radiography 7300 C; Model Number: 712037; Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2... Class II Philips Medical Systems DMC GmbH
May 19, 2021 DigitalDiagnost 4 Flex / Value. radiography and fluoroscopy system Following a system restart where the Table Height 2 (TH2) is the default setting and then switche... Class II Philips Medical Systems DMC GmbH
May 19, 2021 DigitalDiagnost C90 Flex/Value/Chest/ER. radiography and fluoroscopy system Following a system restart where the Table Height 2 (TH2) is the default setting and then switche... Class II Philips Medical Systems DMC GmbH
May 19, 2021 DigitalDiagnost C90 High Performance. radiography and fluoroscopy system Following a system restart where the Table Height 2 (TH2) is the default setting and then switche... Class II Philips Medical Systems DMC GmbH
May 19, 2021 ProxiDiagnost N90. radiography and fluoroscopy system Following a system restart where the Table Height 2 (TH2) is the default setting and then switche... Class II Philips Medical Systems DMC GmbH
May 19, 2021 DigitalDiagnost 4 High Performance. radiography and fluoroscopy system Following a system restart where the Table Height 2 (TH2) is the default setting and then switche... Class II Philips Medical Systems DMC GmbH

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.