PearMatrix P-15 Peptide Enhanced Bone Graft recallZ-1165-2026 · Cerapedics, Inc. · initiated Dec 29, 2025
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Cerapedics, Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Incorrect expiration date
FDA root cause category: Labeling Change Control
What the company is doing
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.
Recall details
- Recall number
- Z-1165-2026
- Status
- Open, Classified
- Initiated by the company
- Dec 29, 2025
- Posted by the FDA
- Jan 23, 2026
- Recalling firm
- Cerapedics, Inc.
- Quantity
- 237 units
- Product code
- NOX
- FDA submissions
- P240001
- 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.
Product description
PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010
Code information (models, lots, serial numbers)
Lot: 7014819/UDI: (01)00850001680196
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- PearlMatrix P-15 Peptide Enhanced Bone Graft, 1.0cc 730-010Cerapedics Inc. · Filler, Bone Void, Synthetic Peptide1 recall0 reports
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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