TemporaryFDAOngoing
Can cause harm that is usually temporary.
Ventriculostomy Kit, REF: 46154
Check the device or its packaging for
UDI-DI: 00673978947396, Lot: 2025-08779
- Why
- 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.
- Distributed
- 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.
- Company
- Medtronic Neurosurgery
- Announced
- This is the date the recall was announced. A company may have started it weeks earlier.
- Recall began
Source: FDA record Z-2768-2026 · retrieved 21 July 2026
Read the official notice