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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-2101-2021 - Cortoss Bone Augmentation Material 10cc Cartridge, Catalog Number 2101-0010, GTIN 00808232000979 2 07/20/2021 FEI # 3004024955
Stryker Spine
Z-2100-2021 - Cortoss Bone Augmentation Material 5cc Cartridge, Catalog Number 2101-0005, GTIN 00808232000962 2 07/20/2021 FEI # 3004024955
Stryker Spine
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