← All recalls
Medical Device

Ventriculostomy Kit, REF: 46154

Recall date: 2026-07-29 · Source: FDA_DEVICE
Brand / Firm
Medtronic Neurosurgery
Product
Ventriculostomy Kit, REF: 46154
Reason for recall
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.
Units affected
167
Description
Ventriculostomy Kit, REF: 46154
View official recall notice →