Burnsville, MN, United States
Apothecary Products, LLC recalls
1 recall recorded since 2018, most recently on 30 March 2023. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 30 March 2023
- Reason
- 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.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-1702-2023, Z-1703-2023
- Eye and Ear Dropper, Product Code 67082
- Medicine Dropper, Product Code K508
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.