Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cortoss Bone Augmentation Material Recalled by Howmedica Osteonics Corp. Due to Shipments were transported outside of the required refrigerated...
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 Howmedica Osteonics Corp. directly.
Affected Products
Cortoss Bone Augmentation Material, Catalog Nos. 2101-0005 and 2101-0010
Quantity: 115
Why Was This Recalled?
Shipments were transported outside of the required refrigerated temperature conditions. Potential hazards if used include nerve damage resulting in paralysis and increased potential for embolism.
Where Was This Sold?
US distribution to California Colorado Florida Georgia Illinois Indiana Kansas Michigan Ohio Pennsylvania Texas Utah Virginia Washington Wisconsin
About Howmedica Osteonics Corp.
Howmedica Osteonics Corp. has 229 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report