# FDA recall Z-1703-2023

> **Apothecary Products, LLC** · Class II · device recall initiated 2023-03-30.

## Product

Medicine Dropper, Product Code K508

## Reason for recall

Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb.

## Distribution

Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, FL, HI, IL, IN, MO, NC, NJ, NY, OK, OR, PA, TN, TX, UT, WA and the country of Canada.

## Key facts

- **Recall number:** Z-1703-2023
- **Recalling firm:** Apothecary Products, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-03-30
- **Report date:** 2023-06-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Burnsville, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1703-2023

## Citation

> AI Analytics. FDA recall Z-1703-2023. Retrieved 2026-07-09 from https://api.ai-analytics.org/recall/Z-1703-2023. Source: US FDA. Licensed CC0.

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