FDA Device recall Z-1056-2022
putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010, PUTTY
- FDA Device
- Class III
- terminated
- Published 2022-05-18
On 2022-05-18 the FDA classified a Class III recall of putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010, PUTTY by Cerapedics, citing patient chart label contains incorrect Part Number and volume amount.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1056-2022 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2022-04-14 |
| Published | 2022-05-18 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Cerapedics |
| Distribution | US |
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.
Identifiers
| code_info | Model/Catalog Number: 700-010 UDI Code: (01)00850001680004(17)240531(10)21C0991 Lot Number: 21C0991 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1056-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.