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Zimmer Biomet Handle For Percutaneous Threaded Drill Guides
No active recall
Manufacturer: Zimmer Biomet · FDA product code: FZX · Category: Guide, Surgical, Instrument
Severity Snapshot
28 total reports2013-03 – 2025-08 date range28.6% physician / facility reported71.4% manufacturer reported2 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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