FDA Device recall Z-2455-2012
***REF LS7600***Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source
- FDA Device
- Class II
- terminated
- Published 2012-10-03
On 2012-10-03 the FDA classified a Class II recall of ***REF LS7600***Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source by Linvatec, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2455-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2011-05-20 |
| Published | 2012-10-03 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Linvatec |
| Distribution | US |
Product
***REF LS7600***Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source
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.
Identifiers
| code_info | GCT |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2455-2012%22
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