Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
ZCORE Porcine Xenograft Particulate in Syringe Product Intended for use Recalled by Collagen Matrix Inc Due to The distributor, Osteogenics Biomedical, notified the firm that...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Collagen Matrix Inc directly.
Affected Products
ZCORE Porcine Xenograft Particulate in Syringe Product Intended for use in dental surgery such as: -Augmentation or reconstructive treatment of alveolar ridge -filling of defects after root resection, apicoectomy and cystectomy -Filling of extraction sockets to enhance preservation of the alveolar ridge -elevation of maxillary sinus floor -Filling of periodontal defects in conjunction with products -Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR) -Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration.
Quantity: 200 units
Why Was This Recalled?
The distributor, Osteogenics Biomedical, notified the firm that the syringes were not working properly and the syringes were being held in quarantine.
Where Was This Sold?
This product was distributed to 1 state: TX
About Collagen Matrix Inc
Collagen Matrix Inc has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report