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.
Incorrect expiration date
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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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.
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.
This recall is not part of a broader industry pattern.
This recall affects patients and healthcare providers by necessitating the immediate cessation of use of the graft, potentially delaying surgical procedures and treatment plans.
The lot number and expiration date can typically be found on the product's packaging or label.
Expect a refund or replacement processing time of approximately 4-6 weeks after the manufacturer receives the returned product.
Keep records of your purchase, including receipts, product packaging, and any correspondence with the manufacturer regarding the recall.
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.
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