Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K061718 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Multi-Drug iCup Drug Screen Test Cup. Part Number DUE-1127-022-08A. Subsequent Product Codes: DI... | 2 | 10/06/2009 |
FEI # 1000125596 Biosite Inc |
| Multi-Drug iCup Drug Screen Test Cup. Part Number DUD-197-014-08A. Subsequent Product Codes: DIO... | 2 | 10/06/2009 |
FEI # 1000125596 Biosite Inc |
| Multi-Drug iCup Drug Screen Test Cup. Part Number DUD-1107-012-08A. Subsequent Product Codes: D... | 2 | 10/06/2009 |
FEI # 1000125596 Biosite Inc |
| Multi-Drug 8 Panel Integrated iCup Drug Screen Test Cup. Part Number DUE-187-071-08A. Subsequent... | 2 | 10/06/2009 |
FEI # 1000125596 Biosite Inc |
| Multi-Drug 8 Panel Integrated iCup Drug Screen Test Cup. Part Number DUD-187-013-08A. Subsequent... | 2 | 10/06/2009 |
FEI # 1000125596 Biosite Inc |
| Calloway LabsMulti-Drug 9 Panel Assay A rapid, one step screening test for the simultaneous for ... | 2 | 07/27/2011 |
FEI # 1000125596 Alere San Diego |
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