Medical Device Recalls
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1 result found
Recall Number: Z-1040-2017 |
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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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| AutoMate 2500 Family Catalog No. ODL25120 AutoMate 1200, ODL25125, AutoMate 1250, ODL25250 AutoMate ... | 3 | 01/18/2017 |
FEI # 2050012 Beckman Coulter Inc. |
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