FDAMarch 30, 2022device
Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage. The kit includes 3 trials. Orthopedic manual surgical instrument
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Product labeled incorrectly. The lot was labeled with Small footprint when the product was Medium.
What to do
FDA enforcement status: Terminated
Brands named
restor3d
UPCs
00840097504506
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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