L-Varlock Cage/Trial Implant Holder recall
L-Varlock Cage/Trial Implant Holder, Reference HD0060, Kisco International, France. Product Usage: The L-Varlock Lumbar Cage is indicated for…
Why was L-Varlock Cage/Trial Implant Holder recalled?
Firm received a complaint of the tip holder breaking during use.
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?
Batch number: 15486
- Product
- L-Varlock Cage/Trial Implant Holder, Reference HD0060, Kisco International, France. Product Usage: The L-Varlock Lumbar Cage is indicated for…
- Recalling firm
- Kiscomedica S.A.
- Quantity
- 13 units
- Distribution
- Worldwide Distribution - US Nationwide in the states of MO and country of Switzerland.
- Recall date
- March 22, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)