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U.S. Department of Health and Human Services

Medical Device Recalls

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41 to 50 of 59 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0524-2016 - ProScreen 5 Panel Dip Card w/Adult, Item No. PSDA-5MB300 3 12/24/2015 Ameditech Inc
Z-0525-2016 - ProScreen 6 Panel Cassette w/Adult (AU), Item No. PSPA-6MBAU 3 12/24/2015 Ameditech Inc
Z-0526-2016 - ProScreen 6 Panel Cup w/Adult (AU), Item No. PSCupA-6MBAU 3 12/24/2015 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 Ameditech Inc
Z-0528-2016 - ProScreen 6 Panel Dip Card w/Adult (AU), Item No. PSDA-6MBAU 3 12/24/2015 Ameditech Inc
Z-0529-2016 - ProScreen 6 Panel Dip Drug Screen, Item No. PSD-6BUPO3 3 12/24/2015 Ameditech Inc
Z-0530-2016 - ProScreen 7 Panel Dip Card, Item No. PSD-7MPB, PSD-7MO, PSD-7M 3 12/24/2015 Ameditech Inc
Z-0531-2016 - ProScreen 8 Panel Dip Card, Item No. PSD-8P 3 12/24/2015 Ameditech Inc
Z-0532-2016 - ProScreen 8 Panel Dip Card w/Adult, Item No. PSDA-8P, PSDA-8MBO300 3 12/24/2015 Ameditech Inc
Z-0533-2016 - ProScreen 8 Panel Dip Card w/Adult, Item No. PSDA-8P, PSDA-8MBO300 3 12/24/2015 Ameditech Inc
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