Medical Device Recalls
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31 to 40 of 59 Results
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-0516-2016 - ProScreen 10 Panel Cup, Item No. PSCup-10M | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0515-2016 - ProScreen 10 Drug Panel Cassette Test, Item No. PSP-10PPX | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0517-2016 - ProScProScreen 10 Panel Cup with Adulterants, Item No. PSCupA-10AM | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0514-2016 - Micro Screen 6 Panel Cup with Adult (AU), Item No. MSCA-6MBAU | 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 |
| 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-0508-2016 - Immutest 11 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-11OP | 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-0512-2016 - ImmuTest Cup 7-panel w/ Adulteration, Item No. IMCA-7P | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
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