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-0524-2016 - ProScreen 5 Panel Dip Card w/Adult, Item No. PSDA-5MB300 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0525-2016 - ProScreen 6 Panel Cassette w/Adult (AU), Item No. PSPA-6MBAU | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0526-2016 - ProScreen 6 Panel Cup w/Adult (AU), Item No. PSCupA-6MBAU | 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 |
| Z-0528-2016 - ProScreen 6 Panel Dip Card w/Adult (AU), Item No. PSDA-6MBAU | 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-0530-2016 - ProScreen 7 Panel Dip Card, Item No. PSD-7MPB, PSD-7MO, PSD-7M | 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 |
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