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BD Bard-Parker
No active recall
Manufacturer: BD · FDA product code: GES · Category: Blade, Scalpel
Severity Snapshot
139 total reports1997-11 – 2025-08 date range8.9% physician / facility reported91.1% 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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