Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010 Recalled by Cerapedics, Inc. Due to Patient chart label contains incorrect Part Number and...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Cerapedics, Inc. directly.
Affected Products
putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010, PUTTY
Quantity: 572 units
Why Was This Recalled?
Patient chart label contains incorrect Part Number and volume amount.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Cerapedics, Inc.
Cerapedics, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report