Z-2455-2012 Class II Terminated
FDA device recall Z-2455-2012 was initiated by Linvatec Corp. Dba ConMed Linvatec on May 20, 2011 and is designated Class II. Reason for recall: 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… The recall status is terminated (terminated Sep 26, 2012). Affected quantity: 1.
Recall Details
- Product Type
- Devices
- Report Date
- Oct 3, 2012
- Initiation Date
- May 20, 2011
- Termination Date
- Sep 26, 2012
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1
Product Description
***REF LS7600***Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source
Reason for Recall
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.
Distribution Pattern
Worldwide Distribution - US Nationwide and the countries of Canada, DK, HK, IN, IT, KR, MY, RU, CO, VN, ZA.
Code Information
GCT
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2455-2012
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026