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Browse Device Recalls

12 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 12 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 12 FDA device recalls.

Clear
DateProductReasonClassFirm
Sep 5, 2025 AW Server 2.0, AW Server 3.0, AW Server 3.1, AW Server 3.2 Firm has identified a security vulnerability in AW Server products. If exploited, a malicious act... Class II GE Medical Systems, SCS
Mar 18, 2024 GE Healthcare Allia IGS 5 Pulse, Interventional fluoroscopic x-ray systems GE HealthCare has become aware of the potential that adhesive material might not have been applie... Class II GE Medical Systems, SCS
Mar 18, 2024 GE Healthcare Innova IGS 6, Interventional fluoroscopic x-ray systems GE HealthCare has become aware of the potential that adhesive material might not have been applie... Class II GE Medical Systems, SCS
Mar 18, 2024 GE Healthcare Allia IGS 7, Interventional fluoroscopic x-ray systems GE HealthCare has become aware of the potential that adhesive material might not have been applie... Class II GE Medical Systems, SCS
Mar 18, 2024 GE Healthcare Innova IGS 5, computed tomography x-ray system GE HealthCare has become aware of the potential that adhesive material might not have been applie... Class II GE Medical Systems, SCS
Mar 18, 2024 GE Healthcare Allia IGS 5 Pulse, Interventional fluoroscopic x-ray systems GE HealthCare has become aware of the potential that adhesive material might not have been applie... Class II GE Medical Systems, SCS
Mar 18, 2024 GE Healthcare Interact Discovery RT, Interventional fluoroscopic x-ray systems GE HealthCare has become aware of the potential that adhesive material might not have been applie... Class II GE Medical Systems, SCS
Mar 18, 2024 GE Healthcare Allia IGS 7 OR, Interventional fluoroscopic x-ray systems GE HealthCare has become aware of the potential that adhesive material might not have been applie... Class II GE Medical Systems, SCS
Dec 26, 2023 Senographe Pristina X-ray exposure termination audible signal on Senographe Pristina with Efficiency Suite 2 intermit... Class II GE Medical Systems, SCS
Mar 29, 2018 Discovery IGS 740 Interventional Fluoroscopic X-ray Systems The Discovery IGS and Innova IGS systems may experience X-ray abort errors which could result in ... Class II GE Medical Systems, SCS
Mar 29, 2018 Discovery IGS 730 Interventional Fluoroscopic X-ray Systems The Discovery IGS and Innova IGS systems may experience X-ray abort errors which could result in ... Class II GE Medical Systems, SCS
Mar 29, 2018 Innova IGS 630/520/530/540 Interventional Fluoroscopic X-ray Systems The Discovery IGS and Innova IGS systems may experience X-ray abort errors which could result in ... Class II GE Medical Systems, SCS

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.