Z-1165-2026 Class II Ongoing

Recalled by Cerapedics, Inc. — Westminster, CO

FDA device recall Z-1165-2026 was initiated by Cerapedics, Inc. on December 29, 2025 and is designated Class II. Reason for recall: Incorrect expiration date The recall status is ongoing. Affected quantity: 237 units.

Recall Details

Product Type
Devices
Report Date
February 4, 2026
Initiation Date
December 29, 2025
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
237 units

Product Description

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

Reason for Recall

Incorrect expiration date

Distribution Pattern

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.

Code Information

Lot: 7014819/UDI: (01)00850001680196