Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

***REF LS7600***Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source Recalled by Linvatec Corp. dba ConMed Linvatec Due to Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated...

Date: May 20, 2011
Company: Linvatec Corp. dba ConMed Linvatec
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Linvatec Corp. dba ConMed Linvatec directly.

Affected Products

***REF LS7600***Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source

Quantity: 1

Why Was This Recalled?

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.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Linvatec Corp. dba ConMed Linvatec

Linvatec Corp. dba ConMed Linvatec has 21 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report