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Lina Loop
No active recall
FDA product code: KNF · Category: Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)
Severity Snapshot
24 total reports2009-07 – 2011-08 date range4.8% physician / facility reported95.2% manufacturer reported2 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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