Medical Device Recalls
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1 result found
510(K) Number: K981580 |
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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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Aeroset Direct HDL Reagent, LN 7D67-01 | 3 | 05/09/2003 | Abbott Laboratories Diagnostic Div |
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