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Stryker Maestro Drill
No active recall
Manufacturer: Stryker · FDA product code: HBB · Category: Motor, Drill, Pneumatic
Severity Snapshot
356 total reports2005-04 – 2022-04 date range0.3% physician / facility reported99.7% manufacturer reported3 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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