Medtronic Neurosurgery recalls

Medtronic Neurosurgery has 32 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 29 Jul 2026. 19 are still ongoing. 1 was reported in the last 12 months.

Total recalls32since 2013
Last 12 months1reported
Class I1341% of total
Ongoing19latest 29 Jul 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 13 41%Class II 19 59%Class III 0 0%

Why medtronic neurosurgery is recalled

By year

Ongoing medtronic neurosurgery recalls

19 active

All medtronic neurosurgery recalls, newest first

32 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIVentriculostomy Kit recalled by Medtronic NeurosurgeryMedtronic NeurosurgeryOtherNationwide
DeviceCLASS IBecker External Drainage and Monitoring System recalledMedtronic NeurosurgeryPackaging DefectsNationwide
DeviceCLASS IExacta External Drainage and Monitoring System recalledMedtronic NeurosurgeryPackaging DefectsNationwide
DeviceCLASS IMedtronic Duet External Drainage and Monitoring System recalledMedtronic NeurosurgeryOtherNationwide
DeviceCLASS IMedtronic Duet External Drainage and Monitoring System recalledMedtronic NeurosurgeryOtherNationwide
DeviceCLASS IMedtronic Duet External Drainage and Monitoring System recalledMedtronic NeurosurgeryOtherNationwide
DeviceCLASS IMedtronic Duet External Drainage and Monitoring System recalledMedtronic NeurosurgeryOtherNationwide
DeviceCLASS IMedtronic Duet External Drainage and Monitoring System recalledMedtronic NeurosurgeryOtherNationwide
DeviceCLASS IIMedtronic REF 46915 Duet External Drainage and Monitoring system recalledMedtronic NeurosurgeryOtherNationwide
DeviceCLASS IIDurepair Dura Regeneration Matrix: Durepair Dura Substitute recalledMedtronic NeurosurgeryOtherNationwide
DeviceCLASS IIMedtronic Delta CSF (Cerebro Spinal Fluid) -Flow Control recalledMedtronic NeurosurgeryOtherNationwide
DeviceCLASS IIMedtronic PS Medical Cerebro Spinal Fluid recalledMedtronic NeurosurgeryOtherNationwide
DeviceCLASS IIMedtronic Cerebro Spinal Fluid Flow Control Valves and Shunts recalledMedtronic NeurosurgeryOtherNationwide
DeviceCLASS IIREF 27219-1 X1, Medtronic, Delta Valve, Neonatal, Performance Level recalledMedtronic NeurosurgeryDevice MalfunctionNationwide
DeviceCLASS IIREF 27219-5 X1, Medtronic, Delta Valve, Neonatal, Performance Level recalledMedtronic NeurosurgeryDevice MalfunctionNationwide
DeviceCLASS IIREF 27219-2 X1, Medtronic, Delta Valve, Neonatal, Performance Level recalledMedtronic NeurosurgeryDevice MalfunctionNationwide
DeviceCLASS IIMedtronic Ares Antibiotic-Impregnated Catheter recalledMedtronic NeurosurgerySterilityNationwide
DeviceCLASS IIMedtronic Ares Antibiotic-Impregnated Catheter recalledMedtronic NeurosurgerySterilityNationwide
DeviceCLASS IIMedtronic Ares Antibiotic-Impregnated Catheter recalledMedtronic NeurosurgerySterilityNationwide
DeviceCLASS IIMedtronic Clip Gun Magazines recalled by Medtronic NeurosurgeryMedtronic NeurosurgerySterility38 states
DeviceCLASS IIModel #: CG8900, Medtronic Clip Gun Scalp Clip Kit (Qty 1); Model # recalledMedtronic NeurosurgeryPackaging DefectsCA
DeviceCLASS IThe Medtronic StrataMR adjustable valves recalledMedtronic NeurosurgeryOtherNationwide
DeviceCLASS IIMedtronic Strata II / Strata NSC Valves recalledMedtronic NeurosurgeryOtherNationwide
DeviceCLASS IMedtronic Duet External Drainage and Monitoring System recalledMedtronic NeurosurgeryOtherPR
DeviceCLASS IMedtronic Duet External Drainage and Monitoring System recalledMedtronic NeurosurgeryOtherPR
DeviceCLASS IMedtronic Duet External Drainage and Monitoring System recalledMedtronic NeurosurgeryOtherPR
DeviceCLASS IMedtronic Duet External Drainage and Monitoring System recalledMedtronic NeurosurgeryOtherPR
DeviceCLASS IMedtronic Duet External Drainage and Monitoring System recalledMedtronic NeurosurgeryOtherPR
DeviceCLASS IICSF-Unitized Shunt, Contoured Regular, Low Pressure recalledMedtronic NeurosurgeryOtherNationwide
DeviceCLASS IIMedtronic Strata II Shunt Assembly Kit, Small recalledMedtronic NeurosurgeryOtherNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.