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Recall Observatory FDA recall evidence

Device product

***REF LS7600***Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source

Z-2455-2012

May 20, 2011

Class II

Product summary

Firm
Linvatec Corp. dba ConMed Linvatec
Event
Event 63009
Status
Terminated
Classification
Class II
Quantity
1
Official record key
device-enforcement:Z-2455-2012

Official wording

Reason: 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.

Code information: GCT

Distribution pattern: Worldwide Distribution - US Nationwide and the countries of Canada, DK, HK, IN, IT, KR, MY, RU, CO, VN, ZA.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.