NeuroMAUDE
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Terumo 19 5 X 86 X 1

No active recall

Manufacturer: Terumo  · FDA product code: GFA  · Category: Blade, Saw, General & Plastic Surgery, Surgical

Severity Snapshot

18 total reports2018-052024-01 date range0% physician / facility reported100% 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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