Bone Graft Recall: Cerapedics PearMatrix P-15 1.0cc REF 730-010
Announced 2026-02-04 · FDA
FDA recall of PearMatrix P-15 1.0cc REF 730-010 Bone Graft due to an incorrect expiration date. A total of 237 units were distributed nationwide across multiple states (CA, CO, CT, FL, GA, ID, IL, KS, LA, MI, MN, MO, MT, NE, NJ, NV, NY, OH, OR, PA, TN, TX, WA, WY). Recall number Lot: 7014819 with UDI (01)00850001680196.
| Brand | Cerapedics, Inc. |
|---|---|
| Product | PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010 |
| Reason | Incorrect expiration date |
| Severity | moderate |
| Units affected | 237 |
| 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. |
| Agency | FDA |
| Recall / campaign no. | Lot: 7014819/UDI: (01)00850001680196 |
WHAT YOU SHOULD DO
- If you have PearMatrix P-15 1.0cc from Lot 7014819, stop using it and contact your healthcare provider.
- Do not implant or administer the product; arrange return or disposal with your facility or distributor.
- If you had a procedure with this product or notice any issues, monitor your health and report adverse events to your clinician and FDA MedWatch.
- For questions, contact the supplying facility, Cerapedics, or FDA recall information for Lot 7014819 / UDI (01)00850001680196.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.