FDA recall, , Moderate risk
Cerapedics PearMatrix P-15 Peptide Enhanced Bone Graft
The bone graft has an incorrect expiration date.
Summary by Recall Canary from the FDA notice
What happened
Cerapedics, Inc., of Westminster, Colorado, recalled PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010, because the product has an incorrect expiration date. The FDA added the recall to its Enforcement Report on January 23, 2026, and the company began the recall on December 29, 2025.
The product was distributed nationwide in 24 states, including 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 and Wyoming.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the UDI-DI and lot code listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010
- UDI-DI
- 00850001680196
- Lot code
- 7014819
Recall details
- Company began the recall
- Sold in
US Nationwide distribution in the states of 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.
- Company
- Cerapedics, Inc.Westminster, Colorado
- Hazard
- Labeling error
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98242
- Recall number
- Z-1165-2026
- Quantity recalled
- 237 units
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
