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Cerapedics, Inc. recalls putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010, PUTTY
Recalled May 18, 2022 · FDA recall Z-1056-2022 · Cerapedics
Hazard
Patient chart label contains incorrect Part Number and volume amount. · FDA Class III
Units
572 units
Sold at
U.S. Nationwide distribution in the states of AL, AZ, CA, CT, DC, DE, ID, IN, KS, KY, MD, MI, MN, MO, NC, NV, NY, OH, PA, TX, VA, and WA.
Description
Patient chart label contains incorrect Part Number and volume amount.
Product
putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010, PUTTY
Manufacturer(s)
Cerapedics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →