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Bard Gammatile
No active recall
Manufacturer: Bard · FDA product code: KXK · Category: Source, Brachytherapy, Radionuclide
Severity Snapshot
11 total reports2020-11 – 2023-03 date range81.8% physician / facility reported18.2% 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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