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U.S. Department of Health and Human Services

Medical Device Recalls

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51 to 60 of 500 Results *
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Product Description
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Recall
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DrugSmart 11 Test Cup, Item No. 61127D 3 Dec-24-2015 Ameditech Inc
DrugSmart 12 Test Cup (Multi & BUP), Item No. 61210D DrugSmart 12 Test Cup (Multi/Single/BUP), Item... 3 Dec-24-2015 Ameditech Inc
DrugSmart 9 Test Cup (BUP), Item No. 60960D 3 Dec-24-2015 Ameditech Inc
DrugSmart Cup 10, Item No. 61093D-3C, 61085D, 61015D 3 Dec-24-2015 Ameditech Inc
DrugSmart Cup THC/COC/AMP//MET/OPI2/BZO, Item No. 60600D 3 Dec-24-2015 Ameditech Inc
DrugSmart Dip (MET/OPI2)+AMP+BZO+COC+THC, Item No. 30600D 3 Dec-24-2015 Ameditech Inc
DrugSmart Dip AMP/OPI2/COC/THC/BZO Test, Item No. 30520D 3 Dec-24-2015 Ameditech Inc
EDI BZO Uncut Sheet - Cup*, Item No. 160170 3 Dec-24-2015 Ameditech Inc
iCup DX 10 Panel w/Adulterant, Item No. I-DXA-1107-142 3 Dec-24-2015 Ameditech Inc
iCup DX 11 Panel w/ Adulterant, Item No. I-DXA-1117-131 3 Dec-24-2015 Ameditech Inc

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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