CLASS II ONGOING Device recall · Reported 4 Feb 2026 · FDA Enforcement Report
PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc recalled
Cerapedics is recalling PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc, distributed nationwide in the US. The recall was initiated on 29 Dec 2025 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1165-2026
- FDA event ID
- 98242
- Recalling firm
- Cerapedics, Westminster, CO
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 29 Dec 2025
- FDA classified
- 23 Jan 2026
- Reported
- 4 Feb 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 29 Dec 2025 | Recall initiated by company | |
| 23 Jan 2026 | Classified by FDA | +25 days |
| 4 Feb 2026 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Incorrect expiration date
Product as listed by the FDA
PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010
Where it was distributed
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.
Nationwide CaliforniaColoradoConnecticutFloridaGeorgiaIdahoIllinoisKansasLouisianaMichiganMinnesotaMissouriMontanaNebraskaNew JerseyNevadaNew YorkOhioOregonPennsylvania
Questions about this recall
Why was it recalled?
Incorrect expiration date
Which lots are affected?
Lot: 7014819/UDI: (01)00850001680196
Where was it 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.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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