Howmedica Osteonics Corp. recalls Cortoss Bone Augmentation Material, Catalog Nos. 2101-0005 a
Recalled Product
Cortoss Bone Augmentation Material, Catalog Nos. 2101-0005 and 2101-0010
Hazard / Issue
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.
Issued by
FDA
Distribution: US distribution to California Colorado Florida Georgia Illinois Indiana Kansas Michigan Ohio Pennsylvania Texas Utah Virginia Washington Wisconsin
Lot/Code Info: Specific shipments of 2101-0005: Lots A1907006, A1908003; 2101-0010: Lots A1903054, A1906006. UDI 00808232000962, 00808232000979
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