Every recall we track for Medtronic Neurosurgery — 21 in all — plus the complaints and injury reports the public filed about them.
Medtronic Neurosurgery recalls Ventriculostomy Kit REF 461: endotoxin levels may exceed safe limits for cerebrospinal fluid contact, causing inflammation. Affected units sold with UDI-DI 00673978947396 and Lot 2025-08779.
Medtronic recalls Becker External Drainage and Monitoring Systems with cracks or leaks in stopcocks. Affected models include EDMS 24146, EDMS II 25120, and others. Stop using if cracks or leaks are present.
Medtronic recalls Exacta External Drainage and Monitoring Systems with cracks or leaks in stopcocks due to complaints. Affected units include specific model numbers and lot numbers listed in the recall notice.
Medtronic recalls Duet External Drainage System with potential catheter disconnection from patient line. Affected units have specific lot numbers. Stop using immediately to prevent serious complications.
Medtronic recalls Duet External Drainage System with potential catheter disconnection from patient line stopcock connectors. Affected units have specific lot numbers. Stop using immediately if you have this device.
Medtronic recalls specific lumbar catheter models due to potential disconnection from patient lines. This could lead to cerebrospinal fluid leakage. Affected units have unique lot numbers; check your device for the listed serial codes.
Medtronic recalls Duet External Drainage System (SmartSite) with potential catheter disconnection from patient line stopcock connectors. Affected units have specific lot numbers. Contact Medtronic for details.
Medtronic recalls Duet External Drainage System with potential catheter disconnection from patient line stopcock connectors. Affected units have specific lot numbers.
Medtronic recalls Duet External Drainage and Monitoring system with incorrect expiration date labeling. Affected units may have safety risks due to outdated expiration dates.
Medtronic recalls Durepair Dura Regeneration Matrix products with potential endotoxin levels that may cause infection-like symptoms. Affected items include specific sizes and expiration dates listed in the recall notice.
Medtronic recalls specific CSF flow control valves for hydrocephalus treatment due to potential variation in radiopaque marking visibility under X-rays.
Medtronic recalls specific CSF flow control valves for hydrocephalus treatment due to potential variation in radiopaque marking visibility under X-ray. Affected models include 22011 L, 22011 M, 22017 B, and others. No immediate action required but check if your valve matches the list.
Medtronic recalls STRATA II shunts and valves for hydrocephalus treatment due to potential variation in radiopaque marking visibility under X-ray imaging. Affected models include specific CFNs and lot numbers listed in the recall.
Medtronic recalls neonatal Delta Valve shunt components due to potential disconnection causing shunt malfunction. Affected units include specific lot numbers for neonatal CSF flow control systems.
Medtronic recalls neonatal Delta Valve shunt components due to potential disconnection causing shunt malfunction. Affected units include specific lot numbers for neonatal CSF flow control systems.
Medtronic recalls neonatal Delta Valve shunt components due to potential shunt malfunction from improper valve connection. Affected units have a shorter ventricular catheter connection site than designed.
Medtronic recalls Ares Antibiotic-Impregnated Catheters with potential seal defects that could compromise sterility, increasing infection risk after hydrocephalus surgery.
Medtronic recalls specific Ares Antibiotic-Impregnated Catheters (REF 91101) due to potential seal defects that could compromise sterility and increase infection risk after hydrocephalus surgery.
Medtronic recalls specific Ares Antibiotic-Impregnated Catheters (REF 95001) due to potential seal defects that could compromise sterility and increase infection risk after hydrocephalus surgery.
Medtronic recalls Clip Gun Magazines with potentially undetected packaging seal breaches that could compromise sterility during surgery. Affected units have specific lot numbers and are sold in sealed pouches.
Medtronic recalls specific scalp clip kits due to inadequate packaging performance. Affected models and lots may not meet current safety standards. Consumers should check their product details and follow official instructions.
