Stryker, Inc. recalls Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238
Recalled Product
Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
Hazard / Issue
The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: UDI: (01)00815742002386/Lot Number(s): 0000228865 0000370674
View official government recall
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