Light Source, Endoscope, Xenon Arc
FDA adverse event reports and recall history for light source, endoscope, xenon arc (product code GCT), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 2,283
- Deaths
- 5
- Injuries
- 87
- Malfunctions
- 2,143
Reports per year
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
- 2012-09-25TerminatedNonconforming Material/Component
***REF LS7600***Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source
Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of their products LS7700 Xenon Universal Light Source and LS7600 Xenon Light Source are intended to be used with an endoscope to provide illumination during endoscopic procedures.
- 2012-09-25TerminatedNonconforming Material/Component
***REF LS7700***Qty 1*** EC REP*** ConMed Linvatec Xenon Universal Light Source
Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of their products LS7700 Xenon Universal Light Source and LS7600 Xenon Light Source are intended to be used with an endoscope to provide illumination during endoscopic procedures.
- 2005-09-10TerminatedNonconforming Material/Component
Linvatec LS 7500, 300 Watt Xenon Light Source Catalog Numbers: LS7500, LS7500L (loaner), LS7500R (refurbished)
Through the complaint handling system, the company has determine there are performance issued involving the LS7500, 300 Watt Xenon Light Source. The performance issues result in a low light output that can create poor illumination of the surgical site.
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