Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cortoss Bone Augmentation Material 10cc Cartridge Recalled by Stryker Spine Due to The products experienced a 12-hour excursion from the...
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 Stryker Spine directly.
Affected Products
Cortoss Bone Augmentation Material 10cc Cartridge, Catalog Number 2101-0010, GTIN 00808232000979
Quantity: 559 total
Why Was This Recalled?
The products experienced a 12-hour excursion from the required refrigerated temperature conditions at the distribution center prior to distribution.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Spine
Stryker Spine has 29 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report