***REF LS7700***Qty 1*** EC REP*** ConMed Linvatec recall
***REF LS7700***Qty 1*** EC REP*** ConMed Linvatec Xenon Universal Light Source
Why was ***REF LS7700***Qty 1*** EC REP*** ConMed Linvatec 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
GCT
- Product
- ***REF LS7700***Qty 1*** EC REP*** ConMed Linvatec Xenon Universal Light Source
- Recalling firm
- Linvatec Corp. dba ConMed Linvatec
- Quantity
- 57
- Distribution
- Worldwide Distribution - US Nationwide and the countries of Canada, DK, HK, IN, IT, KR, MY, RU, CO, VN, ZA.
- Recall date
- October 3, 2012
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)