Medical Device Recalls
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1 result found
Recall Number: Z-3001-2018 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| iView DAB Detection Kit w/o Secondary Antibody, Catalog Number 05266173001, Model 760-093. For l... | 1 | 09/14/2018 |
FEI # 1000125183 Ventana Medical Systems Inc |
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