FDAFDA · Food and drugs·Recall number Z-2455-2012
***REF LS7600***Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source
Published October 3, 2012 · Recall initiated: May 20, 2011
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- Linvatec Corp. dba ConMed Linvatec
- Distributor
- Worldwide Distribution - US Nationwide and the countries of Canada, DK, HK, IN, IT, KR, MY, RU, CO, VN, ZA.
- Lot
- GCT
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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