Ameditech recalls

Ameditech has 109 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 7 Oct 2020.

Total recalls109since 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 7 Oct 2020

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 46 42%Class III 63 58%

Why ameditech is recalled

By year

All ameditech recalls, newest first

109 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IICLIA Waived Rapid Drug Test (AMT recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IIFirst Check 1 Panel Drug Cup: (THC) recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IIFastect¿ II Drug Screen Dipstick Test Single Drug Detection (AMT recalledAmeditechPotency & AssayNationwide
DeviceCLASS IIAlere iCup Drug Detection (AMT recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IIMicroScreen (AMT recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IIOratect III Oral Fluid Drug Screen Device (AMT recalled by AmeditechAmeditechOtherNationwide
DeviceCLASS IIMicroTox (AMT recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IIAlere iScreen Multi Drug Detection (AMT recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IIAlere iScreen Single Drug Detection (AMT recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IIFirst Check 4 Panel Drug Cup: COC/MET1000/OPI2000/THC): (THC/COC) recalledAmeditechPotency & AssayNationwide
DeviceCLASS IIProScreen" Drugs of Abuse Test (AMT recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IIQuickTox Drug Screen DipCard(AMT recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IIFirst Check 2 Panel Drug Cup: (THC/COC) recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IIiCup Dx14 Drug Screen Cup(AMT recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IIToxCup Drug Screen Cup (AMT recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IIConsult Diagnostics Drugs Abuse Test Cup (AMT recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IIFirst Check 14 Panel Drug Cup: (BMC style) recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IIHenry Schein One Step + DOA Cup (AMT recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IITDDA Drugs of Abuse Cup(AMT recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IIDrug Screening Component: Uncut Sheets recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IIImmuTest Drugs of Abuse Cup (AMT recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IINoble 1 Step+ Cup (AMT recalled by AmeditechAmeditechPotency & AssayNationwide
DeviceCLASS IIFirst Check 7 Panel Drug Cup: (AMP/COC/MDMA/MET/OPI/PCP/THC) recalledAmeditechPotency & AssayNationwide
DeviceCLASS IIIQuickTox 5 Panel Drug Screen DipCard recalled by AmeditechAmeditechOther13 states
DeviceCLASS IIIAccutest Drug Test Cup 5+3 recalled by AmeditechAmeditechPackaging DefectsCA
DeviceCLASS IIIAlere iScreen Dx Urine Drug Screen Card recalled by AmeditechAmeditechOther9 states
DeviceCLASS IIIAlere iScreen Dx Urine Drug Screen Card, 20 Drug Detection recalledAmeditechOtherNationwide
DeviceCLASS IIIProScreen 6 Panel Cassette w/Adult (AU) recalled by AmeditechAmeditechOtherNationwide
DeviceCLASS IIIEDI BZO Uncut Sheet - Cup* recalled by AmeditechAmeditechOtherNationwide
DeviceCLASS III6 Panel Cup Body and Lid w/Adult (AU) recalled by AmeditechAmeditechOtherNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.