PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft recall (Cerapedics, Inc.)
Medical deviceClass IIOngoing
Summary: Cerapedics, Inc. is recalling PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010. Reason: Incorrect expiration date.
What is being recalled
PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010
Why
Incorrect expiration date
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
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. (states named: California, Colorado, Connecticut, Florida, Georgia, Idaho, Illinois, Kansas, Louisiana, Michigan, Minnesota, Missouri, Montana, Nebraska, New Jersey, Nevada, New York, Ohio, Oregon, Pennsylvania, Tennessee, Texas, Washington, Wyoming)
How to tell if yours is affected
Lot: 7014819/UDI: (01)00850001680196
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-1165-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | December 29, 2025 |
| Reported | February 4, 2026 |
| Company | Cerapedics, Inc. |
| Company location | Westminster, CO, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 237 units |
More recalls from Cerapedics, Inc. · all medical device recalls · recalls from December 2025