Stryker, Inc. recalls Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
- Recall date
- December 6, 2023
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1084-2024
- 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 Pro 18 Microcatheter, REF 90238 0.021in X150cm
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