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Bard Recovery Cone Removal
No active recall
Manufacturer: Bard · FDA product code: GAE · Category: Snare, Surgical
Severity Snapshot
46 total reports2007-11 – 2017-05 date range6.5% physician / facility reported93.5% 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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