# FDA recall Z-1969-2019

> **Pharmaceutical Innovations, Inc.** · Class II · device recall initiated 2019-06-19.

## Product

ElectroMist product codes: 36-3310-25 - Product Usage: Electrode conductivity spray solution.

## Reason for recall

Potential for failed stability antimicrobial effectiveness testing.

## Distribution

US nationwide distribution including the states of AZ, CA, CT, FL,  IL,  MA, MI, MN, NC, NJ, NY, OH, PA, RI, TX, TN, VT, WV.    Distributed Internationally to accounts in Australia, France, Germany, Hong Kong, Saudi Arabia and Canada.

## Key facts

- **Recall number:** Z-1969-2019
- **Recalling firm:** Pharmaceutical Innovations, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-06-19
- **Report date:** 2019-07-24
- **Termination date:** 2020-07-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Newark, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1969-2019

## Citation

> AI Analytics. FDA recall Z-1969-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1969-2019. Source: US FDA. Licensed CC0.

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