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Aesculap Long Scalpel Handle
No active recall
Manufacturer: Aesculap · FDA product code: GDZ · Category: Handle, Scalpel
Severity Snapshot
19 total reports2017-02 – 2024-12 date range42.1% physician / facility reported57.9% 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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