Medtronic Neurosurgery recalls
Every recall we track for Medtronic Neurosurgery — 21 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Medtronic Neurosurgery dropped to zero in 2025 (0, down from 7 in 2024). 5% rated “stop using now”.
All FDA recall records for Medtronic Neurosurgery since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 1 | 0 | 1 |
| 2018 | 0 | 0 | 1 | 0 | 1 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 5 | 1 | 0 | 6 |
| 2021 | 0 | 0 | 3 | 0 | 3 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 1 | 1 | 2 |
| 2024 | 1 | 6 | 0 | 0 | 7 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 1 | 0 | 1 |
What to do if you have a recalled Medtronic Neurosurgery product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Medtronic Neurosurgery recalls
10 shown- Lower riskMedical device
Medtronic Neurosurgery recalls Ventriculostomy Kit, REF: 46154
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.
Medtr: NeurosurgeryJun 17, 2026 - Use cautionMedical device
Medtronic Neurosurgery recalls Exacta External Drainage and Monitoring System: 27581 KIT 27581 EXACTA W/EDM VCATH 35CM 27636 EDM 27636 EXACTA
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 NeurosurgeryNov 1, 2024 - Use cautionMedical device
Medtronic Neurosurgery recalls Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, REF 46913, Sterile EO, Rx Only. Used
Medtronic recalls Duet External Drainage System with potential catheter disconnection from patient line stopcock connectors. Affected units have specific lot numbers.
MedtronicJan 22, 2024 - Lower riskMedical device
Medtronic Neurosurgery recalls Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter,
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 NeurosurgeryJun 28, 2023 - UnratedMedical device
Medtronic Neurosurgery recalls Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2, 61100; DUREPAIR DURA SUBSTITUTE 3 X 3, 61105;
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 NeurosurgeryJun 13, 2023 - Lower riskMedical device
Medtronic Neurosurgery recalls Medtronic Cerebro Spinal Fluid Flow Control Valves and Shunts. STRATA II Valves and Shunts for the following CFNs:
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.
MedtronicJan 11, 2021 - Use cautionMedical device
Medtronic Neurosurgery recalls REF 27219-2 X1, Medtronic, Delta Valve, Neonatal, Performance Level 2.0, CE 0344, Sterile EO - Product Usage: Neonatal
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.
MedtronicDec 16, 2020 - Use cautionMedical device
Medtronic Neurosurgery recalls Medtronic Ares Antibiotic-Impregnated Catheter, REF: 95001, Sterile, Rx Only. Used in the treatment of hydrocephalus as
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.
MedtronicDec 8, 2020 - Lower riskMedical device
Medtronic Neurosurgery recalls Medtronic Clip Gun Magazines are packaged in individually sealed pouches and distributed in boxes containing 5
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.
MedtronicMay 3, 2018 - Lower riskMedical device
Medtronic Neurosurgery recalls Model #: CG8900, Medtronic Clip Gun Scalp Clip Kit (Qty 1); Model #: CG8901, Medtronic Clip Gun Scalp Clip Kit (Qty
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.
MedtronicDec 20, 2017
Medtronic Neurosurgery recall questions
How many recalls has Medtronic Neurosurgery had?
21 recalls from Medtronic Neurosurgery are on record with U.S. safety agencies, from 2017–2026.
What is the most recent Medtronic Neurosurgery recall?
Medtronic Neurosurgery recalls Ventriculostomy Kit, REF: 46154, dated Jun 17, 2026. Every Medtronic Neurosurgery recall is listed on this page, newest first.
What should I do if I have a recalled Medtronic Neurosurgery product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Medtronic Neurosurgery recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.