Medical Device Recalls
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1 result found
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-2692-2014 - ABX PENTRA Magnesium RTU Reagent, Part No. A11A01646 Product Usage: ABX PENTRA Magnesium RTU reagent with associated calibrators and controls are for quantitative in vitro diagnostic determination... | 2 | 09/24/2014 |
FEI # 3002698356 Horiba Instruments, Inc dba Horiba Medical |
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