Linvatec Corp. dba ConMed Linvatec: Medical Device Recall in 2012 - (Recall #: Z-2455-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: May 20, 2011

Date Posted: October 3, 2012

Recall Number: Z-2455-2012

Event ID: 63009

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.

Status: Terminated

Product Quantity: 1

Code Information:

GCT

Distribution Pattern:

Worldwide Distribution - US Nationwide and the countries of Canada, DK, HK, IN, IT, KR, MY, RU, CO, VN, ZA.

Voluntary or Mandated:

Voluntary: Firm initiated