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Open, Classified

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

FDA Recall Z-1165-2026 · Posted 2026-01-23

Recalling FirmCerapedics, Inc.
Recall StatusOpen, Classified
Product CodeNOX
Date Initiated2025-12-29
Product Quantity237 units

Reason for Recall

Incorrect expiration date

Firm Action

On December 29, 2025, Cerapedics issues a "Urgent: Medical Device Recall" notification to affected consignees via Email. Cerapedics asked consignees to take the following actions: 1. Please immediately examine your inventory and return any remaining units of PearlMatrix 1.0cc, lot 7014819. " RMA will be issued for this return and a shipping label. 2. Please acknowledge receipt of this letter by responding to this email or call toll-free at 1-866-360-5612. 3. If you have further distributed this product, please identify your customers, and notify them at once of this product recall. You may provide a copy of this recall notification letter to your customer.

Root Cause

Labeling Change Control

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.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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