Stryker, Inc. recalls Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm
- Recall date
- December 6, 2023
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1085-2024
- FDA classification
- Class II
- Brand / firm
- Stryker, Inc.
- Sold / distributed
- US Nationwide distribution in the states of AL, FL, GA, HI, IL, MI, NC, NH, OH, PA, TX, VA.
Why it was recalled
The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm
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