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Terumo Power Pro
No active recall
Manufacturer: Terumo · FDA product code: GFA · Category: Blade, Saw, General & Plastic Surgery, Surgical
Severity Snapshot
11 total reports2009-04 – 2010-04 date range0% physician / facility reported100% 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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