Class III — Cerapedics, Inc.
| Recalling firm | Cerapedics, Inc. |
|---|---|
| Registered facility | Cerapedics, Inc. (the firm's only registered facility) |
| Classification | Class III |
| Status | Terminated |
| Reason | 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 |
| Quantity | 572 units |
| Distribution | 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. |
| Initiated | 2022-04-14 |
| Classified | 2022-05-10 |
| Terminated | 2024-12-23 |
| Recall number | Z-1056-2022 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class III recall — Cerapedics, Inc. (Z-1056-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/90015/
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