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Browse Device Recalls

31 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 31 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 31 FDA device recalls.

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DateProductReasonClassFirm
Nov 1, 2024 Becker External Drainage and Monitoring System: 24146 EDMS 24146 BECKER NO Y... Due to complaints received reporting cracks and/or leaks of the stopcocks associated with the ext... Class I Medtronic Neurosurgery
Nov 1, 2024 Exacta External Drainage and Monitoring System: 27581 KIT 27581 EXACTA W/EDM... Due to complaints received reporting cracks and/or leaks of the stopcocks associated with the ext... Class I Medtronic Neurosurgery
Jan 22, 2024 Medtronic Duet External Drainage and Monitoring System, Interlink Injection S... Potential for catheter disconnection from the patient line stopcock connectors. Class I Medtronic Neurosurgery
Jan 22, 2024 Medtronic Duet External Drainage and Monitoring System, SmartSite Injection S... Potential for catheter disconnection from the patient line stopcock connectors. Class I Medtronic Neurosurgery
Jan 22, 2024 Medtronic Duet External Drainage and Monitoring System, Interlink Injection S... Potential for catheter disconnection from the patient line stopcock connectors. Class I Medtronic Neurosurgery
Jan 22, 2024 Medtronic Duet External Drainage and Monitoring System, SmartSite, Injection ... Potential for catheter disconnection from the patient line stopcock connectors. Class I Medtronic Neurosurgery
Jan 22, 2024 Medtronic Duet External Drainage and Monitoring System, Interlink Injection S... Potential for catheter disconnection from the patient line stopcock connectors. Class I Medtronic Neurosurgery
Jun 28, 2023 Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink I... Product labeling contains incorrect expiration date Class II Medtronic Neurosurgery
Jun 13, 2023 Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2, 61100; ... Dura regeneration matrix may have out-of-specification endotoxin levels due to issues with in-pro... Class II Medtronic Neurosurgery
Jan 11, 2021 Medtronic Delta CSF (Cerebro Spinal Fluid) -Flow Control Valves for the foll... Potential for variation in radiopaque marking visibility under radiographic imaging for adjustabl... Class II Medtronic Neurosurgery
Jan 11, 2021 Medtronic PS Medical Cerebro Spinal Fluid (CSF)-Flow Control Valves for the... Potential for variation in radiopaque marking visibility under radiographic imaging for adjustabl... Class II Medtronic Neurosurgery
Jan 11, 2021 Medtronic Cerebro Spinal Fluid Flow Control Valves and Shunts. STRATA II V... Potential for variation in radiopaque marking visibility under radiographic imaging for adjustabl... Class II Medtronic Neurosurgery
Dec 16, 2020 REF 27219-1 X1, Medtronic, Delta Valve, Neonatal, Performance Level 1.0, CE ... Neonatal Valves were manufactured with a ventricular catheter connection site shorter than the de... Class II Medtronic Neurosurgery
Dec 16, 2020 REF 27219-5 X1, Medtronic, Delta Valve, Neonatal, Performance Level 1.5, CE ... Neonatal Valves were manufactured with a ventricular catheter connection site shorter than the de... Class II Medtronic Neurosurgery
Dec 16, 2020 REF 27219-2 X1, Medtronic, Delta Valve, Neonatal, Performance Level 2.0, CE ... Neonatal Valves were manufactured with a ventricular catheter connection site shorter than the de... Class II Medtronic Neurosurgery
Dec 8, 2020 Medtronic Ares Antibiotic-Impregnated Catheter, REF: 93092, Sterile, Rx Only.... There is a potential for a defect on the seal of the outer pouch of catheters. The defect may com... Class II Medtronic Neurosurgery
Dec 8, 2020 Medtronic Ares Antibiotic-Impregnated Catheter, REF: 91101, Sterile, Rx Only.... There is a potential for a defect on the seal of the outer pouch of catheters. The defect may com... Class II Medtronic Neurosurgery
Dec 8, 2020 Medtronic Ares Antibiotic-Impregnated Catheter, REF: 95001, Sterile, Rx Only.... There is a potential for a defect on the seal of the outer pouch of catheters. The defect may com... Class II Medtronic Neurosurgery
May 3, 2018 Medtronic Clip Gun Magazines are packaged in individually sealed pouches and ... The packaging sterile barrier does not comply with the applicable packaging standard for terminal... Class II Medtronic Neurosurgery
Dec 20, 2017 Model #: CG8900, Medtronic Clip Gun Scalp Clip Kit (Qty 1); Model #: CG8901, ... Medtronic is initiating a voluntary recall because the products identified above did not adequate... Class II Medtronic Neurosurgery
Feb 22, 2017 The Medtronic StrataMR adjustable valves and shunts are designed to provide c... Incorrect valve rotor orientation due to misalignment and/or off-center positioning of the Strata... Class I Medtronic Neurosurgery
Jan 17, 2017 Medtronic Strata II / Strata NSC Valves (includes Burr Hole and Lumbar Perito... Medtronic Neurosurgery initiated a recall after receiving five (5) Product Experiences between Fe... Class II Medtronic Neurosurgery
Jun 9, 2014 Medtronic Duet External Drainage and Monitoring System, Interlink Injection S... Medtronic Neurosurgery is recalling the Medtronic Duet External Drainage and Monitoring Systems b... Class I Medtronic Neurosurgery
Jun 9, 2014 Medtronic Duet External Drainage and Monitoring System, SmartSite Injection S... Medtronic Neurosurgery is recalling the Medtronic Duet External Drainage and Monitoring Systems b... Class I Medtronic Neurosurgery
Jun 9, 2014 Medtronic Duet External Drainage and Monitoring System, Interlink Injection S... Medtronic Neurosurgery is recalling the Medtronic Duet External Drainage and Monitoring Systems b... Class I Medtronic Neurosurgery
Jun 9, 2014 Medtronic Duet External Drainage and Monitoring System, Interlink Injection S... Medtronic Neurosurgery is recalling the Medtronic Duet External Drainage and Monitoring Systems b... Class I Medtronic Neurosurgery
Jun 9, 2014 Medtronic Duet External Drainage and Monitoring System, SmartSite Injection S... Medtronic Neurosurgery is recalling the Medtronic Duet External Drainage and Monitoring Systems b... Class I Medtronic Neurosurgery
Nov 18, 2013 CSF-Unitized Shunt, Contoured Regular, Low Pressure, Catalog No. 46022; CSF-... Medtronic Neurosurgery is recalling the CSF-Unitized Shunts, Delta Shunt Assembly Kit, and the St... Class II Medtronic Neurosurgery
Nov 18, 2013 Medtronic Strata II Shunt Assembly Kit, Small, Catalog No. 27848. Strata ... Medtronic Neurosurgery is recalling the CSF-Unitized Shunts, Delta Shunt Assembly Kit, and the St... Class II Medtronic Neurosurgery
Nov 18, 2013 Medtronic Delta Shunt Assembly Kit with Bioglide Small, Performance Level 1.0... Medtronic Neurosurgery is recalling the CSF-Unitized Shunts, Delta Shunt Assembly Kit, and the St... Class II Medtronic Neurosurgery
Jun 28, 2013 Medtronic Preimplantation Test Kit, Catalog No. 21047. The kit is indicated f... Medtronic Neurosurgery is recalling the Medtronic Preimplantation Test Kit because the outer cart... Class II Medtronic Neurosurgery

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.