Recall Z-1056-2022— Cerapedics, Inc.

Name: FDA recall Z-1056-2022
Creator: U.S. Food and Drug Administration
Published: 2022-04-14

Class III · Terminated

Class III FDA medical device recall by Cerapedics, Inc., initiated 2022-04-14, terminated 2024-12-23. FDA's recall record names no specific 510(k) clearance for this event. Product: putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010, PUTTY. Reason: Patient chart label contains incorrect Part Number and volume amount..

Recalling firm: Cerapedics, Inc.
Classification: Class III
Status: Terminated
Initiated: 2022-04-14
Terminated: 2024-12-23
Firm location: Westminster, CO, United States

Product description

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

Reason for recall

Patient chart label contains incorrect Part Number and volume amount.

Data sourced from openFDA. This site is unofficial and independent of the FDA.