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Stockert Radiofrequency Ablation Generator
No active recall
FDA product code: GXD · Category: Generator, Lesion, Radiofrequency
Severity Snapshot
88 total reports2004-07 – 2005-07 date range0% physician / facility reported100% 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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