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Stryker X6000 Xenon Lightsource
No active recall
Manufacturer: Stryker · FDA product code: GCT · Category: Light Source, Endoscope, Xenon Arc
Severity Snapshot
15 total reports2001-07 – 2009-12 date range0% physician / facility reported100% 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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