FDAApril 14, 2022device
putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010, PUTTY
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Patient chart label contains incorrect Part Number and volume amount.
What to do
FDA enforcement status: Terminated
Brands named
cerapedics
UPCs
00850001680004
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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