Medical Device Recalls
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11 to 20 of 59 Results
Related Medical Device Recalls |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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|---|---|---|---|
| Z-0535-2016 - ProScreen CLIA Waived Cup 6 Drugs w/Adul, Item No. PSCupA-6MB-W | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0537-2016 - ProScreen CLIA Waived Cup with 8 Drug, Item No. PSCup-8P-W | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0536-2016 - ProScreen CLIA Waived Cup with 6 Drugs, Item No. PSCup-6BO-W | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0534-2016 - ProScreen 9 Panel Cup w/Adulterants, Item No. PSCUPA-9BO300 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0531-2016 - ProScreen 8 Panel Dip Card, Item No. PSD-8P | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0532-2016 - ProScreen 8 Panel Dip Card w/Adult, Item No. PSDA-8P, PSDA-8MBO300 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0533-2016 - ProScreen 8 Panel Dip Card w/Adult, Item No. PSDA-8P, PSDA-8MBO300 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0530-2016 - ProScreen 7 Panel Dip Card, Item No. PSD-7MPB, PSD-7MO, PSD-7M | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0529-2016 - ProScreen 6 Panel Dip Drug Screen, Item No. PSD-6BUPO3 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0527-2016 - ProScreen 6 Panel Dip Card, Item No. PSCuPSD-6BUP300, PSD-6MTDBO300, PSD-6BUPO, PSD-6MBO, PSD-6MB, | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
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