FDA Medical devices recall ·
PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc recall
- Recall number
- Z-1165-2026
- Date
- (initiated December 29, 2025)
- Company / brand
- Cerapedics, Inc.
11025 Dover St Unit 1600, Westminster, CO, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 237 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010
Why was it recalled?
Incorrect expiration date
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot: 7014819/UDI: (01)00850001680196
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.
States: 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
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1165-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.