***REF LS7700***Qty 1*** EC REP*** ConMed Linvatec Xenon Universal… — Class II medical device recall Z-2456-2012
Terminated recall by Linvatec Corp. dba ConMed Linvatec, reported 2012-10-03, distributed nationwide. Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of their products LS7700 Xenon Universa
| Recall number | Z-2456-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Linvatec Corp. dba ConMed Linvatec, Largo, FL, United States |
| Recall initiated | 2011-05-20 |
| Classified | 2012-09-25 |
| Reported by FDA | 2012-10-03 |
| Terminated | 2012-09-26 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 57 |
Product
***REF LS7700***Qty 1*** EC REP*** ConMed Linvatec Xenon Universal 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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2456-2012. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.