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Lina Gold Loop
No active recall
FDA product code: KNF · Category: Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)
Severity Snapshot
22 total reports2010-11 – 2024-01 date range14.3% physician / facility reported85.7% 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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