Ameditech Inc: 26 recalls on record

Recalls filed with 1 agency: FDA (26).

First recall on record: October 22, 2014. Most recent: October 7, 2020.

Risk classification: Class II: 11 · Class III: 15

Most recent recalls

DateAgencyProduct
October 7, 2020FDATDDA Drugs of Abuse Cup(AMT Item/ AMT Description): TDDA-6MBAU-CUP /"TDDA Drugs of Abu…Z-3044-2020
October 7, 2020FDAImmuTest Drugs of Abuse Cup (AMT Item Number/ AMT Description): IMCA-5AB-W / "ImmuTest…Z-3036-2020
October 7, 2020FDANoble 1 Step+ Cup (AMT Item Number/ AMT Description): NBCA-13A-B /"Noble 1 Step + Cup"…Z-3039-2020
October 7, 2020FDAFirst Check 7 Panel Drug Cup: (AMP/COC/MDMA/MET/OPI/PCP/THC); AMT Item Number 990100BZ-3050-2020
October 7, 2020FDADrug Screening Component: Uncut Sheets Part Number/ Description/ LOT Number 100163/ EDI…Z-3051-2020
December 30, 2015FDAiCup DX 12 Panel w/ Adulterant, Item No. I-DXA-1127-023Z-0504-2016
December 30, 2015FDADrugSmart Cup 10, Item No. 61093D-3C, 61085D, 61015DZ-0497-2016
December 30, 2015FDAImmutest 12 Panel Cup w/Adulteration, Item No. IMCA-11OPZ-0510-2016
December 30, 2015FDA10-Panel Pipette Drug Screen, Item No. PSP-10MZ-0485-2016
December 30, 2015FDABZO Strip Dip Card (300ng/ml)*, Item No. 100170Z-0490-2016
December 30, 2015FDAImmutest 10 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-10M5Z-0507-2016
December 30, 2015FDAProScreen CLIA Waived Cup with 6 Drugs, Item No. PSCup-6BO-WZ-0536-2016
December 30, 2015FDAImmutest 5 Pnl Drug Cup w/ Adult -waived, Item No. IMCA-5AB-WZ-0509-2016
December 30, 2015FDADrugSmart 11 Test Cup, Item No. 61127DZ-0494-2016
December 30, 2015FDAProScreen Cup CLIA with 6 Panel Drug, Item No. PSCup-6MB-WZ-0539-2016
December 30, 2015FDA1 Step 12 Panel Cup, Item No. NBCA-12M-WZ-0484-2016
December 30, 2015FDAProScreen 10 Drug Panel Cassette Test, Item No. PSP-10PPXZ-0515-2016
December 30, 2015FDAProScreen 12 Drug Cup w/Adulteration, Item No. PSCupA-12TBUZ-0520-2016
December 30, 2015FDA11 Panel Card (OPI 300) w/Adult, Item No. 71125AAZ-0487-2016
December 30, 2015FDAImmuTest Cup 7-panel w/ Adulteration, Item No. IMCA-7PZ-0512-2016
November 25, 2015FDA12-Panel Dip Drug Screen with adulterant, Item No. PSDA-12BUP These Drugs of Abuse Tests…Z-0302-2016
November 25, 2015FDA11 Panel Dip Card (OPI 2000), Item No. 11125AA2K; 11 Panel Dip Card (OPI 300) w/Adult, It…Z-0301-2016
November 25, 2015FDA10-Panel Pipette Drug Screen, Item No. PSP-10M These Drugs of Abuse Tests are one-step i…Z-0299-2016
October 22, 2014FDAArcPoint Labs 10 Panel Dip Screen (BAR), Part No. APD-10M. The ArcPoint Labs Dip Drug …Z-0072-2015
October 22, 2014FDAArcPoint Labs 10 Panel Dip Screen (OXY), Part No. APD-10MO. The ArcPoint Labs Dip Drug…Z-0073-2015

Questions about this company

How many recalls does Ameditech Inc have?
Recalert has 26 U.S. recalls on record for Ameditech Inc, published between October 22, 2014 and October 7, 2020.
What was the most recent Ameditech Inc recall?
FDA recall Z-3044-2020, published October 7, 2020: TDDA Drugs of Abuse Cup(AMT Item/ AMT Description): TDDA-6MBAU-CUP /"TDDA Drugs of Abuse Cup AMP300/BZO200/COC300/MET300/OPI300/ THC50 with Cr, Ni, pH, Bl, S.G."
Which agencies have handled Ameditech Inc recalls?
Ameditech Inc appears as the recalling firm in recalls from: FDA (26).

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