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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
Related Medical Device Recalls
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Z-2375-2012 - Omnilife Science Apex Knee System Modular Tibia Augment, Size 6 x 4mm Ref: KC-54060. The Apex Knee System is intended for use as a primary or revision total knee replacement. 2 09/13/2012 FEI # 3008342029
Omni Life Science
Z-2374-2012 - Omnilife Science Apex Knee System Modular Tibia Augment, Size 5 x 4mm Ref: KC-54050. The Apex Knee System is intended for use as a primary or revision total knee replacement. 2 09/13/2012 FEI # 3008342029
Omni Life Science
Z-2373-2012 - Omnilife Science Apex Knee System Modular Tibia Augment, Size 4 x 4mm Ref: KC-54040. The Apex Knee System is intended for use as a primary or revision total knee replacement. 2 09/13/2012 FEI # 3008342029
Omni Life Science
Z-2372-2012 - Omnilife Science Apex Knee System Modular Tibia Augment, Size 3 x 4mm Ref: KC-54030. The Apex Knee System is intended for use as a primary or revision total knee replacement. 2 09/13/2012 FEI # 3008342029
Omni Life Science
Z-2371-2012 - Omnilife Science Apex Knee System Modular Tibia Augment, Size 2 x 4mm Ref: KC-54020. The Apex Knee System is intended for use as a primary or revision total knee replacement. 2 09/13/2012 FEI # 3008342029
Omni Life Science
Z-2370-2012 - Omnilife Science Apex Knee System Modular Tibia Augment, Size 1 x 4mm Ref: KC-54010. The Apex Knee System is intended for use as a primary or revision total knee replacement. 2 09/13/2012 FEI # 3008342029
Omni Life Science
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