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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K113046
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Product Description
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FDA Recall
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ProScreen" Drugs of Abuse Test (AMT Item/ AMT Description): PSD-6MB/ "ProScreen" Drugs of Abuse T... 2 09/30/2020 FEI # 3003789989
Ameditech Inc
Drug Screening Component: Uncut Sheets Part Number/ Description/ LOT Number 100163/ EDI OPI (300) ... 2 09/30/2020 FEI # 3003789989
Ameditech Inc
ArcPoint Labs 10 Panel Dip Screen (BAR), Part No. APD-10M. The ArcPoint Labs Dip Drug Screen Dip ... 2 10/16/2014 FEI # 3003789989
Ameditech Inc
ArcPoint Labs 5 Panel Dip Drug Screen, Part No. APD-5M. The ArcPoint Labs Dip Drug Screen Dip Car... 2 10/16/2014 FEI # 3003789989
Ameditech Inc
ArcPoint Labs 10 Panel Dip Screen (OXY), Part No. APD-10MO. The ArcPoint Labs Dip Drug Screen Dip... 2 10/16/2014 FEI # 3003789989
Ameditech Inc
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