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Stryker, Inc. recalls Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
Recalled February 21, 2024 · FDA recall Z-1084-2024 · Stryker
Hazard
The microcatheter IFU contains an intended use that has not been evaluated by the FDA. · FDA Class II
Units
11 units
Sold at
US Nationwide distribution in the states of AL, FL, GA, HI, IL, MI, NC, NH, OH, PA, TX, VA.
Description
The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
Product
Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
Manufacturer(s)
Stryker, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →