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Stryker Drill Bit 2
No active recall
Manufacturer: Stryker · FDA product code: HTW · Category: Bit, Drill
Severity Snapshot
41 total reports1992-07 – 2026-02 date range13.2% physician / facility reported86.8% manufacturer reported24 SKU variants
Reporting Trend
Annual Reporting Volume
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Note: the 2018 Voluntary Malfunction Summary Reporting expansion means volume increases may reflect surveillance changes, not increased device risk.
Reported Events
Submitted to FDA MAUDE by physicians, hospitals, manufacturers, and patients.
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