Medtronic Neurosurgery recalls Ventriculostomy Kit
- Recalling company
- Medtronic Neurosurgery
- Product
- Ventriculostomy Kit, REF: 46154
- Reason
- Ventriculostomy devices, used during ventriculostomy procedures to gain access to the ventricular system, may exhibit endotoxin levels that exceed the acceptable limit for devices that come into contact with cerebrospinal fluid; endotoxin exposure can cause an acute inflammatory process.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jun 17, 2026
- Reported
- Jul 29, 2026
- Distribution
- Worldwide - US Nationwide distribution in the states of UT, AL, CA, NC, GA, AR, LA, KY, LA, KY, IL, OK and the country of Costa Rica.
- Status
- Ongoing
- Quantity
- 167
- Lot / codes
- UDI-DI: 00673978947396, Lot: 2025-08779
- Company location
- Haltom City, TX
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2768-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2768-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.