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.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0692-2020%22
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