FDAJanuary 11, 2017device
L-Varlock Cage/Trial Implant Holder, Reference HD0060, Kisco International, France. Product Usage: The L-Varlock Lumbar Cage is indicated for intervertebral body fusion procedures in skeletally mature patients with degenerative disc disease (DDD) of the lumbar spine at one or two contiguous level...
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Firm received a complaint of the tip holder breaking during use.
What to do
FDA enforcement status: Terminated
Brands named
kiscomedica
Recall history
No related federal recalls on record for this brand yet.
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