Medical Device Recalls
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11 to 20 of 84 Results
510(K) Number: K113046 |
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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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| CLIA RDTC 12-Panel Cup (w/Adulteration), Item No. CLIA-RDTC-12, DCC-81205-5 | 3 | 12/24/2015 | Ameditech Inc |
| DrugCheck Waived 12 Panel Cup w/Adult, Item No. DCC-81205-5 | 3 | 12/24/2015 | Ameditech Inc |
| DrugSmart 10 Test Cup (PCP & OXY), Item No. 61020D | 3 | 12/24/2015 | Ameditech Inc |
| DrugSmart 11 Test Cup, Item No. 61127D | 3 | 12/24/2015 | Ameditech Inc |
| DrugSmart 12 Test Cup (Multi & BUP), Item No. 61210D DrugSmart 12 Test Cup (Multi/Single/BUP), Item... | 3 | 12/24/2015 | Ameditech Inc |
| DrugSmart 9 Test Cup (BUP), Item No. 60960D | 3 | 12/24/2015 | Ameditech Inc |
| DrugSmart Cup 10, Item No. 61093D-3C, 61085D, 61015D | 3 | 12/24/2015 | Ameditech Inc |
| DrugSmart Cup THC/COC/AMP//MET/OPI2/BZO, Item No. 60600D | 3 | 12/24/2015 | Ameditech Inc |
| DrugSmart Dip (MET/OPI2)+AMP+BZO+COC+THC, Item No. 30600D | 3 | 12/24/2015 | Ameditech Inc |
| DrugSmart Dip AMP/OPI2/COC/THC/BZO Test, Item No. 30520D | 3 | 12/24/2015 | Ameditech Inc |
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