Medical Device Recalls
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Related 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-0484-2016 - 1 Step 12 Panel Cup, Item No. NBCA-12M-W | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0542-2016 - THERMO FISHER 8 DRUG CASSETTE, Item No. MTPA-8MBAU | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0486-2016 - 11 Panel Dip Card (OPI 300) w/Adult, Item No. 11125AA | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0487-2016 - 11 Panel Card (OPI 300) w/Adult, Item No. 71125AA | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0488-2016 - 12-Panel Dip Drug Screen with adulterant, Item No. PSDA-12BUP, PSD-6MTDBO300, PSD-10PPX, PSD-10MOX, 60960D, 61127D, DCC-81205-5, IMCA-10M5. | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0489-2016 - 6 Panel Cup Body and Lid w/Adult (AU), Item No. TDDA-6MBAU-CUP | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0490-2016 - BZO Strip Dip Card (300ng/ml)*, Item No. 100170 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0491-2016 - CLIA RDTC 12-Panel Cup (w/Adulteration), Item No. CLIA-RDTC-12, DCC-81205-5 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0492-2016 - DrugCheck Waived 12 Panel Cup w/Adult, Item No. DCC-81205-5 | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
| Z-0493-2016 - DrugSmart 10 Test Cup (PCP & OXY), Item No. 61020D | 3 | 12/24/2015 |
FEI # 3003789989 Ameditech Inc |
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