Medical Device Recalls
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21 to 30 of 79 Results
510(K) Number: K113501 |
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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 11 Panel w/ Adulterant, Item No. I-DXA-1117-131 | 3 | 12/24/2015 | Ameditech Inc |
| iCup DX 12 Panel w/ Adulterant, Item No. I-DXA-1127-023 | 3 | 12/24/2015 | Ameditech Inc |
| iCup DX 6 Panel w/Adulterant, Item No. I-DXA-167-013 | 3 | 12/24/2015 | Ameditech Inc |
| iCup DX 8 Panel w/Adulterant, Item No. I-DXA-187-016 | 3 | 12/24/2015 | Ameditech Inc |
| Immutest 10 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-10M5 ... | 3 | 12/24/2015 | Ameditech Inc |
| Immutest 11 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-11OP ... | 3 | 12/24/2015 | Ameditech Inc |
| Immutest 5 Pnl Drug Cup w/ Adult -waived, Item No. IMCA-5AB-W ... | 3 | 12/24/2015 | Ameditech Inc |
| Immutest 12 Panel Cup w/Adulteration, Item No. IMCA-11OP ... | 3 | 12/24/2015 | Ameditech Inc |
| ImmuTest 12 Panel Dip Card, Item No. IMD-12MO3 | 3 | 12/24/2015 | Ameditech Inc |
| ImmuTest Cup 7-panel w/ Adulteration, Item No. IMCA-7P ... | 3 | 12/24/2015 | Ameditech Inc |
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