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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 59 Results
Related Medical Device Recalls
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Product Description
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Z-0494-2016 - DrugSmart 11 Test Cup, Item No. 61127D 3 12/24/2015 Ameditech Inc
Z-0495-2016 - DrugSmart 12 Test Cup (Multi & BUP), Item No. 61210D DrugSmart 12 Test Cup (Multi/Single/BUP), Item No. 61205D 3 12/24/2015 Ameditech Inc
Z-0496-2016 - DrugSmart 9 Test Cup (BUP), Item No. 60960D 3 12/24/2015 Ameditech Inc
Z-0497-2016 - DrugSmart Cup 10, Item No. 61093D-3C, 61085D, 61015D 3 12/24/2015 Ameditech Inc
Z-0498-2016 - DrugSmart Cup THC/COC/AMP//MET/OPI2/BZO, Item No. 60600D 3 12/24/2015 Ameditech Inc
Z-0499-2016 - DrugSmart Dip (MET/OPI2)+AMP+BZO+COC+THC, Item No. 30600D 3 12/24/2015 Ameditech Inc
Z-0500-2016 - DrugSmart Dip AMP/OPI2/COC/THC/BZO Test, Item No. 30520D 3 12/24/2015 Ameditech Inc
Z-0501-2016 - EDI BZO Uncut Sheet - Cup*, Item No. 160170 3 12/24/2015 Ameditech Inc
Z-0511-2016 - ImmuTest 12 Panel Dip Card, Item No. IMD-12MO3 3 12/24/2015 Ameditech Inc
Z-0512-2016 - ImmuTest Cup 7-panel w/ Adulteration, Item No. IMCA-7P 3 12/24/2015 Ameditech Inc
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