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Stryker Matrixmandible 1
No active recall
Manufacturer: Stryker · FDA product code: DZI · Category: Drill, Bone, Powered
Severity Snapshot
99 total reports2013-02 – 2026-03 date range39.4% physician / facility reported60.6% manufacturer reported16 SKU variants
Failure & Consequence Profiles
Top Failure Modes
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Top Patient Outcomes
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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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