Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K884968 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ADx Methadone, list 9676-55; Abbott Laboratories, Diagnostics Division, Abbott Park, IL 60064 | 3 | 02/04/2004 | Abbott Laboratories HPD/ADD/GPRD |
| TDx/TDxFLx Methadone, list 9676-60; Abbott Laboratories, Diagnostics Division, Abbott Park, IL 60064 | 3 | 02/04/2004 | Abbott Laboratories HPD/ADD/GPRD |
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