# FDA recall Z-0270-2019

> **Ameditech Inc** · Class III · device recall initiated 2017-09-30.

## Product

Accutest Drug Test Cup 5+3    Product Usage:  The Accutest Drug Test Cup is an in vitro diagnostic test for the rapid detection of multiple drugs in human urine. The test is intended as the first step in a two-step process to provide consumers with information concerning the presence or absence of drugs or their metabolites in a urine sample. Information regarding confirmatory testing- the second step in the process-is provided in the package labeling.

## Reason for recall

Product was released to market without the adulteration strip included in the product.

## Distribution

US in the state of California

## Key facts

- **Recall number:** Z-0270-2019
- **Recalling firm:** Ameditech Inc
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-09-30
- **Report date:** 2018-10-31
- **Termination date:** 2019-08-06

- **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-0270-2019

## Citation

> AI Analytics. FDA recall Z-0270-2019. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0270-2019. Source: US FDA. Licensed CC0.

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