QuickTox 5 Panel Drug Screen DipCard — Class III medical device recall Z-0692-2020
Terminated recall by Ameditech Inc, reported 2019-12-25, distributed in AZ, CA, FL, GA, KS, LA, MI, MO…. Mixed Products containing QuickTox 5 Panel Drugs Screen Dipcard (P/N QT11, LOT #188787) and Alere iScreen Drug
| Recall number | Z-0692-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ameditech Inc, San Diego, CA, United States |
| Recall initiated | 2019-02-15 |
| Classified | 2019-12-17 |
| Reported by FDA | 2019-12-25 |
| Terminated | 2021-04-28 |
| Distributed | AZ, CA, FL, GA, KS, LA, MI, MO, MS, NC, OK, TN, TX |
| Lot numbers | 188787 |
| Model numbers | QT11 |
Product
QuickTox 5 Panel Drug Screen DipCard
Reason for recall
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)
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0692-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.