Quick Facts at a Glance
- Recall Date
- December 29, 2025
- Hazard Level
- HIGH
- Brand
- Cerapedics
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Cerapedics
- Product type
- Bone Graft
- Model numbers
- Lot: 7014819/UDI: (01)00850001680196
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
December 29, 2025
Reported by FDA DEVICE
February 4, 2026
RecallRadar source check
February 11, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Incorrect expiration date
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Cerapedics, Inc. or your healthcare provider for instructions. Notification method: E-Mail
About This Product
The PearMatrix P-15 Peptide Enhanced Bone Graft is used in surgical procedures to promote bone healing by providing a scaffold for new bone growth. Healthcare providers commonly utilize this product in orthopedic and dental surgeries.
Why This Is Dangerous
The hazard arises from the product having an incorrect expiration date, which may compromise its effectiveness and safety when used in medical procedures. Using a product that is past its expiration can lead to suboptimal results or complications for patients.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
This recall affects patients and healthcare providers by necessitating the immediate cessation of use of the graft, potentially delaying surgical procedures and treatment plans.
Practical Guidance
How to identify if yours is affected
- Locate the lot number on your product packaging.
- Verify if your lot number is 7014819.
- Check the expiration date printed on the packaging.
Where to find product info
The lot number and expiration date can typically be found on the product's packaging or label.
What timeline to expect
Expect a refund or replacement processing time of approximately 4-6 weeks after the manufacturer receives the returned product.
If the manufacturer is unresponsive
- Contact the manufacturer directly via email for updates.
- Document all communication attempts regarding your inquiry.
How to prevent similar issues
- Always check expiration dates before using medical devices.
- Research product recalls regularly, especially for medical devices.
- Ensure you purchase medical devices from reputable suppliers.
Documentation advice
Keep records of your purchase, including receipts, product packaging, and any correspondence with the manufacturer regarding the recall.
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Product Details
The recalled product is PearMatrix P-15 Peptide Enhanced Bone Graft, 1.0cc, REF: 730-010. It was distributed nationwide in the United States, including states such as California and New York. The recall involves 237 units.
Key Facts
- Product: PearMatrix P-15 Peptide Enhanced Bone Graft
- Quantity recalled: 237 units
- Hazard: Incorrect expiration date
- Distribution: US Nationwide
- Recall initiated on: December 29, 2025
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Safety Guide
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