# FDA recall Z-3041-2020

> **Ameditech Inc** · Class II · device recall initiated 2020-08-18.

## Product

Oratect III Oral Fluid Drug Screen Device (AMT Item Number/ AMT Description):    HM12-CE	"Oratect¿ III Oral Fluid Drug Screen Device  MET25+THC40+COC20+AMP25+OPI10+BZO5 "

## Reason for recall

XXX

## Distribution

US - Nationwide  OUS - Australia, France, Germany, New Zealand, Singapore and Spain

## Key facts

- **Recall number:** Z-3041-2020
- **Recalling firm:** Ameditech Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-08-18
- **Report date:** 2020-10-07
- **Termination date:** 2024-09-30

- **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-3041-2020

## Citation

> AI Analytics. FDA recall Z-3041-2020. Retrieved 2026-07-06 from https://api.ai-analytics.org/recall/Z-3041-2020. Source: US FDA. Licensed CC0.

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