Class II
Medical Device Recall: Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
Stryker, Inc. · December 6, 2023
Reason for Recall
The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
Distribution
US Nationwide distribution in the states of AL, FL, GA, HI, IL, MI, NC, NH, OH, PA, TX, VA.
States Affected
NATIONWIDE
Quantity Affected
11 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1084-2024
Status: ongoing
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