Medical Device Recalls
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81 to 84 of 84 Results
510(K) Number: K052115 |
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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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| iCup DX 12 Panel w/ Adulterant, Item No. I-DXA-1127-023 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| iCup DX 6 Panel w/Adulterant, Item No. I-DXA-167-013 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| iCup DX 8 Panel w/Adulterant, Item No. I-DXA-187-016 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| iCup Drug Screen Cup, Item No. I-DXA-187-016, I-DXA-167-013; iCup DX 10 Panel w/Adulterant, Item No... | 2 | 11/18/2015 |
FEI # 3003789989 Ameditech Inc |
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