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Zimmer Biomet Dhs® Dcs® Guide Shaft With Flats
No active recall
Manufacturer: Zimmer Biomet · FDA product code: FZX · Category: Guide, Surgical, Instrument
Severity Snapshot
50 total reports2014-02 – 2024-10 date range6% physician / facility reported94% 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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