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Terumo Unknown_Endoscopy_Product
No active recall
Manufacturer: Terumo · FDA product code: GFA · Category: Blade, Saw, General & Plastic Surgery, Surgical
Severity Snapshot
39 total reports2013-03 – 2025-11 date range10.3% physician / facility reported89.7% manufacturer reported1 SKU variants
Failure & Consequence Profiles
Top Failure Modes
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Top Patient Outcomes
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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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