Bone Graft Syringe Recall: Patient Chart Labels List Incorrect Part Numbers
Cerapedics is recalling putty i-FACTOR Peptide Enhanced Bone Graft syringes because patient chart labels contain incorrect Part Numbers and volume amounts. The company discovered the labeling discrepancy in 572 units distributed nationwide.
- Product
- putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010, PUTTY
- Category
- Medical Device
- Distribution
- Distributed nationwide