Home/Recalls/FDA-Z-1165-2026
FDA DevicesClass II

PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010

Published: February 4, 2026Recall ID: Z-1165-2026Category: devicesCountry: US

Reason for Recall / Hazard

Incorrect expiration date

Product Description & Identification

PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010

Affected Products

PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010

Additional Source Details

FieldValue
CityWestminster
StateCO
Event id98242
Address 111025 Dover St Unit 1600
Address 2N/A
Code infoLot: 7014819/UDI: (01)00850001680196
Postal code80021-5574
Report date20260204
Product typeDevices
Product quantity237 units
Reason for recallIncorrect expiration date
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20251229
Initial firm notificationE-Mail
Center classification date20260123

Overview

  • Recalling FirmCerapedics, Inc.
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS 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.
Official Agency Alert