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U.S. Department of Health and Human Services

Medical Device Recalls
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41 to 50 of 84 Results
510(K) Number: K052115
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Product Description
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FDA Recall
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ProScreen 10 Panel Dip Card w/Adult, Item No. PSDA-10MO, PSDA-10MMO300, PSDA-10PPX, PSDA-10BUP, PSD... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ProScreen 12 Drug Cup w/Adulteration, Item No. PSCupA-12TBU ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ProScreen 12 Panel Cup w/Adult., Item No. PSCupA-12M ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ProScreen 12 Panel Dip Card, Item No. PSD-12BUP ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ProScreen 5 Panel Dip Card, Item No. PSD-12BUP ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ProScreen 5 Panel Dip Card w/Adult, Item No. PSDA-5MB300 ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ProScreen 6 Panel Cassette w/Adult (AU), Item No. PSPA-6MBAU ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
ProScreen 6 Panel Cup w/Adult (AU), Item No. PSCupA-6MBAU ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
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
ProScreen 6 Panel Dip Card w/Adult (AU), Item No. PSDA-6MBAU ... 3 12/24/2015 FEI # 3003789989
Ameditech Inc
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