Recall Z-2455-2012— Linvatec Corp. dba ConMed Linvatec
Class II · Terminated
Class II FDA medical device recall by Linvatec Corp. dba ConMed Linvatec, initiated 2011-05-20, terminated 2012-09-26. It names one FDA 510(k) clearance: K070376. 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..
- Recalling firm
- Linvatec Corp. dba ConMed Linvatec
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2011-05-20
- Terminated
- 2012-09-26
- Firm location
- Largo, FL, United States
510(k) clearances named in this recall
1 on FDA's recordK-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.