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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Implants & Prosthetics

PearMatrix P-15 Bone Graft Recalled for Incorrect Expiration Date

Agency Publication Date: January 23, 2026
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Summary

Cerapedics, Inc. is recalling 237 units of PearMatrix P-15 Peptide Enhanced Bone Graft (1.0cc) because the packaging displays an incorrect expiration date. Using a medical device past its intended shelf life could mean the product is no longer as effective or sterile as required for surgery. This recall affects lot 7014819, and consumers or healthcare facilities should contact the manufacturer to arrange for a return or correction.

Risk

The incorrect expiration date may lead to the use of the bone graft after its validated stability period, which could compromise the product's performance or safety during medical procedures.

What You Should Do

  1. This recall affects PearMatrix P-15 Peptide Enhanced Bone Graft (1.0cc) sold under REF 730-010 with lot number 7014819 and UDI (01)00850001680196.
  2. Identify affected units by checking the lot number and UDI printed on the product labeling or outer carton.
  3. Stop using the recalled product immediately.
  4. Contact Cerapedics, Inc. or your distributor to arrange for the return, replacement, or correction of the affected units.
  5. For additional questions, call the FDA at 1-888-463-6332 (1-888-INFO-FDA).

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: PearMatrix P-15 Peptide Enhanced Bone Graft (1.0cc)
Model / REF:
730-010
Lot Numbers:
7014819
UDI:
(01)00850001680196

Recall #: Z-1165-2026

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98242
Status: Active
Manufacturer: Cerapedics, Inc.
Sold By: Hospitals; Surgical Centers; Medical Distributors
Manufactured In: United States
Units Affected: 237 units
Distributed To: California, Colorado, Connecticut, Florida, Georgia, Idaho, Illinois, Kansas, Louisiana, Michigan, Minnesota, Missouri, Montana, Nebraska, New Jersey, Nevada, New York, Ohio, Oregon, Pennsylvania, Tennessee, Texas, Washington, Wyoming

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.