Medical Device Recalls
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Related Medical Device Recalls |
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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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| Z-0504-2016 - iCup DX 12 Panel w/ Adulterant, Item No. I-DXA-1127-023 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0505-2016 - iCup DX 6 Panel w/Adulterant, Item No. I-DXA-167-013 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0506-2016 - iCup DX 8 Panel w/Adulterant, Item No. I-DXA-187-016 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0507-2016 - Immutest 10 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-10M5 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0508-2016 - Immutest 11 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-11OP | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0509-2016 - Immutest 5 Pnl Drug Cup w/ Adult -waived, Item No. IMCA-5AB-W | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0510-2016 - Immutest 12 Panel Cup w/Adulteration, Item No. IMCA-11OP | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0511-2016 - ImmuTest 12 Panel Dip Card, Item No. IMD-12MO3 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0512-2016 - ImmuTest Cup 7-panel w/ Adulteration, Item No. IMCA-7P | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0513-2016 - Immutest Cup CLIA Waived w/Adulteration, Item No. IMCA-7MT-W | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
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