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Bard Parker
No active recall
Manufacturer: Bard · FDA product code: GES · Category: Blade, Scalpel
Severity Snapshot
87 total reports2002-06 – 2022-01 date range8.2% physician / facility reported91.8% 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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