Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2455-2012 — ***REF LS7600***Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source

U.S. FDA — Device Enforcement · United States · 2011-05-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2455-2012
Date of alert
2011-05-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Linvatec Corp. dba ConMed Linvatec
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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