Medtronic Neurosurgery recalls

Recall found. Medtronic Neurosurgery is named in FDA Class II recall Z-2768-2026 covering Ventriculostomy Kit. Hazard: 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. Identifying details: UDI-DI: 00673978947396, Lot: 2025-08779. Status: Ongoing.

Models with recalls

Ventriculostomy Kit (1)

All Medtronic Neurosurgery recalls

FDA Class II · Medical device · July 29, 2026

Ventriculostomy Kit recall — Medtronic Neurosurgery

Ventriculostomy devices, used during ventriculostomy procedures to gain access to the ventricular system, may exhibit endotoxin levels that exceed the acceptable limit for devices …

Official ID Z-2768-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.