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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 84 Results
510(K) Number: K052115
 
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First Check 2 Panel Drug Cup: (THC/COC); AMT Item Number 990600B 2 09/30/2020 FEI # 3003789989
Ameditech Inc
First Check 1 Panel Drug Cup: (THC); AMT Item Number 990400B 2 09/30/2020 FEI # 3003789989
Ameditech Inc
ImmuTest Drugs of Abuse Cup (AMT Item Number/ AMT Description): IMCA-5AB-W / "ImmuTest Drugs of A... 2 09/30/2020 FEI # 3003789989
Ameditech Inc
First Check 4 Panel Drug Cup: COC/MET1000/OPI2000/THC): (THC/COC); AMT Item Number 990100B 2 09/30/2020 FEI # 3003789989
Ameditech Inc
First Check 7 Panel Drug Cup: (AMP/COC/MDMA/MET/OPI/PCP/THC); AMT Item Number 990100B 2 09/30/2020 FEI # 3003789989
Ameditech Inc
CLIA RDTC 12-Panel Cup and CLIA RDTC 12-Panel Cup (w/Adulteration), Item No. CLIA-RDTC-12 These Dru... 2 11/18/2015 FEI # 3003789989
Ameditech Inc
DrugCheck Pipette 10 Drug Test, Item No. 41025 DC These Drugs of Abuse Tests are one-step immunoass... 2 11/18/2015 FEI # 3003789989
Ameditech Inc
DrugCheck Waived 12 Panel Cup w/Adult, Item No. DCC-81205-5 These Drugs of Abuse Tests are one-step... 2 11/18/2015 FEI # 3003789989
Ameditech Inc
DrugSmart 10 Test Cup (PCP & MDMA), Item No. 61055D; DrugSmart 10 Test Cup (PCP & OXY), Item No. 61... 2 11/18/2015 FEI # 3003789989
Ameditech Inc
DrugSmart 11 Test Cup, Item No. 61127D; DrugSmart 12 Test Cup (Multi & BUP), Item No. 61210D; Drug... 2 11/18/2015 FEI # 3003789989
Ameditech Inc
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