Medical Device Recalls
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1 result found
510(K) Number: K802902 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Package Insert for TDx/TDxFLx and TDxFLx Carbamazepine Reagents, REF 9515, item number 69-5121/R4; A... | 2 | 07/20/2004 | Abbott Laboratories HPD/ADD/GPRD |
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