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Medtronic Neurosurgery recalls Ventriculostomy Kit, REF: 46154
Recalled July 29, 2026 · FDA recall Z-2768-2026 · Medtronic Neurosurgery
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. · FDA Class II
Units
167
Sold at
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.
Description
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.
Product
Ventriculostomy Kit, REF: 46154
Manufacturer(s)
Medtronic Neurosurgery
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →