NeuroMAUDE
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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 reports2011-092026-03 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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