Cerapedics, Inc.: Medical Device Recall in 2022 - (Recall #: Z-1056-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010, PUTTY

Product Classification:

Class III

Date Initiated: April 14, 2022

Date Posted: May 18, 2022

Recall Number: Z-1056-2022

Event ID: 90015

Reason for Recall:

Patient chart label contains incorrect Part Number and volume amount.

Status: Terminated

Product Quantity: 572 units

Code Information:

Model/Catalog Number: 700-010 UDI Code: (01)00850001680004(17)240531(10)21C0991 Lot Number: 21C0991

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated