HIGH

Cerapedics Recalls Bone Graft Due to Incorrect Expiration Date

Cerapedics recalled 237 units of PearMatrix P-15 Peptide Enhanced Bone Graft on December 29, 2025. The recall affects products distributed nationwide after a review revealed incorrect expiration dates. Patients and healthcare providers should stop using the product immediately.

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

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

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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.

The Hazard

The recall was initiated due to incorrect expiration dates on the product, potentially compromising its effectiveness. Using a bone graft beyond its expiration date poses health risks for patients undergoing procedures.

Reported Incidents

There are no reported injuries or incidents associated with this product at the time of the recall. However, the incorrect expiration date raises concerns about patient safety.

What to Do

Patients and healthcare providers should stop using the affected product immediately. They should contact Cerapedics, Inc. or their healthcare provider for further instructions regarding the recall.

Contact Information

For more information, contact Cerapedics, Inc. via email. Additional details are available on the FDA's website at the provided link.

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 Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
Lot: 7014819/UDI: (01)00850001680196
Affected States
ALL
Report Date
February 4, 2026
Recall Status
ACTIVE

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