Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AUGMENT Injectable Kit Recalled by BioMimetic Therapeutics, LLC Due to The kit contains the wrong vial tray in...
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 BioMimetic Therapeutics, LLC directly.
Affected Products
AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343
Quantity: 499 units
Why Was This Recalled?
The kit contains the wrong vial tray in the package.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About BioMimetic Therapeutics, LLC
BioMimetic Therapeutics, LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report