Stryker Spine recalls Monterey AL Implant Inserter; 10/12mm; Catalog 48019100.
- Recall date
- February 28, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1488-2025
- FDA classification
- Class II
- Brand / firm
- Stryker Spine
- Sold / distributed
- Domestic: CA, CO, FL, GA, IL, MA, NE, NH, NY, OK, PA, TX, UT. International: Canada.
Why it was recalled
Potential for the gold unlock button to separate from the inserter.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Monterey AL Implant Inserter; 10/12mm; Catalog 48019100.
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