Medical Device Recalls
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1 to 2 of 2 Results
Recall Date to: 04/18/2015 PMA Number: P020055 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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iView DAB Detection Kit, Part number: 760-091 (05266157001) This detection kit is intended for i... | 2 | 07/01/2011 | Ventana Medical Systems Inc |
ultraView Universal DAB Detection Kit, Part number: 760-500 (05269806001) This detection kit is i... | 2 | 07/01/2011 | Ventana Medical Systems Inc |
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