Omni Life Science: 7 recalls on record
Recalls filed with 1 agency: FDA (7).
First recall on record: September 19, 2012. Most recent: November 23, 2016.
Risk classification: Class II: 6 · Class III: 1
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| November 23, 2016 | FDA | OMNIBotics Tracker Kit -Model: RM-10000 The TOTAL KNEE SURGETICS Navigation System wi…Z-0610-2017 | Z-0610-2017 |
| September 19, 2012 | FDA | Omnilife Science Apex Knee System Modular Tibia Augment, Size 3 x 4mm Ref: KC-54030. …Z-2372-2012 | Z-2372-2012 |
| September 19, 2012 | FDA | Omnilife Science Apex Knee System Modular Tibia Augment, Size 5 x 4mm Ref: KC-54050. …Z-2374-2012 | Z-2374-2012 |
| September 19, 2012 | FDA | Omnilife Science Apex Knee System Modular Tibia Augment, Size 1 x 4mm Ref: KC-54010. …Z-2370-2012 | Z-2370-2012 |
| September 19, 2012 | FDA | Omnilife Science Apex Knee System Modular Tibia Augment, Size 6 x 4mm Ref: KC-54060. …Z-2375-2012 | Z-2375-2012 |
| September 19, 2012 | FDA | Omnilife Science Apex Knee System Modular Tibia Augment, Size 4 x 4mm Ref: KC-54040. …Z-2373-2012 | Z-2373-2012 |
| September 19, 2012 | FDA | Omnilife Science Apex Knee System Modular Tibia Augment, Size 2 x 4mm Ref: KC-54020. …Z-2371-2012 | Z-2371-2012 |
Questions about this company
- How many recalls does Omni Life Science have?
- Recalert has 7 U.S. recalls on record for Omni Life Science, published between September 19, 2012 and November 23, 2016.
- What was the most recent Omni Life Science recall?
- FDA recall Z-0610-2017, published November 23, 2016: OMNIBotics Tracker Kit -Model: RM-10000 The TOTAL KNEE SURGETICS Navigation System with iBlock (Now OMNIBotics) is intended for use during stereotaxic surgery to aid the surgeon in locating anato…
- Which agencies have handled Omni Life Science recalls?
- Omni Life Science appears as the recalling firm in recalls from: FDA (7).
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