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Zimmer Biomet Guide Wire 3
No active recall
Manufacturer: Zimmer Biomet · FDA product code: FZX · Category: Guide, Surgical, Instrument
Severity Snapshot
26 total reports2014-11 – 2024-09 date range19.2% physician / facility reported80.8% manufacturer reported1 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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