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Terumo Bone Cutter 5
No active recall
Manufacturer: Terumo · FDA product code: GFA · Category: Blade, Saw, General & Plastic Surgery, Surgical
Severity Snapshot
40 total reports2011-09 – 2026-03 date range2.5% physician / facility reported97.5% 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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