# FDA recall Z-0692-2020

> **Ameditech Inc** · Class III · device recall initiated 2019-02-15.

## 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)

## Distribution

US - AZ, CA, FL, GA, KS, LA, MI, MO, MS, NC, OK, TN, and TX.    OUS - None

## Key facts

- **Recall number:** Z-0692-2020
- **Recalling firm:** Ameditech Inc
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-02-15
- **Report date:** 2019-12-25
- **Termination date:** 2021-04-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Diego, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0692-2020

## Citation

> AI Analytics. FDA recall Z-0692-2020. Retrieved 2026-06-01 from https://api.ai-analytics.org/recall/Z-0692-2020. Source: US FDA. Licensed CC0.

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