Omni Life Science Recall: Omnilife Science Apex Knee System Modular Tibia Augment, Size 5
Omni Life Science Recall: Omnilife Science Apex Knee System Modular Tibia Augment, Size 5 is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Omni Life Science; Product: Omnilife Science Apex Knee System Modular Tibia Augment, Size 5 x 4mm Ref: KC-54050. The Apex Knee System is intended fo
| Recalling firm | Omni Life Science |
|---|---|
| Product | 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. |
| Reason for recall | The Apex Knee System Modular Tibia Augment may breach the inner and outer sterile pouches, compromising the sterility |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Worldwide Distribution-USA (nationwide including the states of CO, NY, OK, PA, UT, VA, and WI, and the countries of Spain and the Netherlands. |
| Recall initiated | 20120809 |
| Recall number | Z-2374-2012 |
| Category | device |
| State | MA |
| Country | United States |
$29/mo
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