Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
BioMend Extend Recalled by Collagen Matrix, Inc. Due to There is a possibility that the product was...
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
BioMend Extend, REF# 0142Z, Synthetic bone grafting material.
Quantity: 569
Why Was This Recalled?
There is a possibility that the product was packaged in the wrong box. Specifically, the product may have been placed inside a BioMend box instead of a BioMend Extend box. The only difference between the two boxes is the product trade name. The label placed on the box and on the product packaged inside the box is correct. The Instructions for Use inside the box are correct.
Where Was This Sold?
Distributed to one distributor located in Florida.
About Collagen Matrix, Inc.
Collagen Matrix, Inc. has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report