Medtronic Neurosurgery recalls Ventriculostomy Kit, REF: 46154
See all recalls from Medtronic Neurosurgery →Recalled Product
Ventriculostomy Kit, REF: 46154
Hazard / Issue
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.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI: 00673978947396, Lot: 2025-08779
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
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