Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Z-0494-2016 - DrugSmart 11 Test Cup, Item No. 61127D | 3 | 12/24/2015 |
FEI # 3003789989 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 |
FEI # 3003789989 Ameditech Inc |
| Z-0496-2016 - DrugSmart 9 Test Cup (BUP), Item No. 60960D | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0497-2016 - DrugSmart Cup 10, Item No. 61093D-3C, 61085D, 61015D | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0498-2016 - DrugSmart Cup THC/COC/AMP//MET/OPI2/BZO, Item No. 60600D | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0499-2016 - DrugSmart Dip (MET/OPI2)+AMP+BZO+COC+THC, Item No. 30600D | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0500-2016 - DrugSmart Dip AMP/OPI2/COC/THC/BZO Test, Item No. 30520D | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0501-2016 - EDI BZO Uncut Sheet - Cup*, Item No. 160170 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0502-2016 - iCup DX 10 Panel w/Adulterant, Item No. I-DXA-1107-142 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0503-2016 - iCup DX 11 Panel w/ Adulterant, Item No. I-DXA-1117-131 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
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