putty i-FACTOR Peptide Enhanced Bone Graft 1 — Class III medical device recall Z-1056-2022
Terminated recall by Cerapedics, Inc., reported 2022-05-18, distributed nationwide. Patient chart label contains incorrect Part Number and volume amount.
| Recall number | Z-1056-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cerapedics, Inc., Westminster, CO, United States |
| Recall initiated | 2022-04-14 |
| Classified | 2022-05-10 |
| Reported by FDA | 2022-05-18 |
| Terminated | 2024-12-23 |
| Distributed | Nationwide (US) |
| Quantity | 572 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00850001680004 |
| Lot numbers | 21C0991 |
| Model numbers | 700-010 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1056-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.