Medical Device Recalls
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1 to 2 of 2 Results
Related Medical Device Recalls |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Z-2717-2011 - iView DAB Detection Kit, Part number: 760-091 (05266157001) This detection kit is intended for in vitro diagnostic use. Ventana Medical Systems' (Ventana) iVIEW DAB Detection Kit is an indirect bi... | 2 | 07/01/2011 |
FEI # 1000125183 Ventana Medical Systems Inc |
| Z-2716-2011 - ultraView Universal DAB Detection Kit, Part number: 760-500 (05269806001) This detection kit is intended for in vitro diagnostic use. Ventana Medical Systems' (Ventana) iVIEW DAB Detection Kit is a... | 2 | 07/01/2011 |
FEI # 1000125183 Ventana Medical Systems Inc |
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