# FDA device recall: Ventriculostomy Kit, REF: 46154

> recall · VERIFIED · 2026-06-17

Firm: Medtronic Neurosurgery · Class II · 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 conta

- Company: Medtronic Neurosurgery
- Sector: medical devices
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.