FDA Device recall Z-0692-2020
QuickTox 5 Panel Drug Screen DipCard
- FDA Device
- Class III
- terminated
- Published 2019-12-25
On 2019-12-25 the FDA classified a Class III recall of QuickTox 5 Panel Drug Screen DipCard by Ameditech, citing mixed Products containing QuickTox 5 Panel Drugs Screen Dipcard (P/N QT11, LOT #188787) and Alere iScreen Drugs of Abuse Dip Test (P/N X11-IS10-22015-DX LOT #188744).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0692-2020 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2019-02-15 |
| Published | 2019-12-25 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Ameditech |
| Distribution | AZ, CA, FL, GA, KS, LA, MI, MO, MS, NC, OK, TN, TX |
Product
QuickTox 5 Panel Drug Screen DipCard
Reason
Mixed Products containing QuickTox 5 Panel Drugs Screen Dipcard (P/N QT11, LOT #188787) and Alere iScreen Drugs of Abuse Dip Test (P/N X11-IS10-22015-DX LOT #188744)
Identifiers
| code_info | Catalog Number: QT11 Lot Number: 188787 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Other recalls by Ameditech
- ToxCup Drug Screen Cup (AMT Item Number/ AMT Description): HT29A/"ToxCup¿ Drug Screen Cup COC300/MET500/OPI300/THC50/AMP1000/PCP25/OXY100 A…
FDA Device · Class II · 2020-10-07 · Ameditech - First Check 4 Panel Drug Cup: COC/MET1000/OPI2000/THC): (THC/COC)
FDA Device · Class II · 2020-10-07 · Ameditech - MicroScreen (AMT Item Number/ AMT Description): MSCA-6MBAU/ "MicroScreen AMP300/BZO200/COC300/MET300/OPI300/ THC50 with Cr, Ni, pH, Bl, S.G…
FDA Device · Class II · 2020-10-07 · Ameditech - TDDA Drugs of Abuse Cup(AMT Item/ AMT Description): TDDA-6MBAU-CUP /"TDDA Drugs of Abuse Cup AMP300/BZO200/COC300/MET300/OPI300/ THC50 with…
FDA Device · Class II · 2020-10-07 · Ameditech - MicroTox (AMT Item Number/ AMT Description): MTPA-6MBAU / "MicroTox (AMP300/BZO200)+(COC300/THC50)+ (MET300/MOR300) With Cr, Ni, pH, Bl, S.…
FDA Device · Class II · 2020-10-07 · Ameditech
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0692-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.