Class II — Cerapedics, Inc.
| Recalling firm | Cerapedics, Inc. |
|---|---|
| Registered facility | Cerapedics, Inc. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Incorrect expiration date |
| Product | PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010 |
| Quantity | 237 units |
| Distribution | US Nationwide distribution in the states of CA, CO, CT, FL, GA, ID, IL, KS, LA, MI, MN, MO, MT, NE, NJ, NV, NY, OH,OR, PA, TN, TX, WA, WY. |
| Initiated | 2025-12-29 |
| Classified | 2026-01-23 |
| Recall number | Z-1165-2026 |
| 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 II recall — Cerapedics, Inc. (Z-1165-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98242/
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