Medicine Dropper, Product Code K508
Reported: June 21, 2023 Initiated: March 30, 2023 #Z-1703-2023
Product Description
Medicine Dropper, Product Code K508
Reason for Recall
Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb.
Details
- Recalling Firm
- Apothecary Products, LLC
- Units Affected
- 1,596 units
- 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.
- Location
- Burnsville, MN
Frequently Asked Questions
What product was recalled? ▼
Medicine Dropper, Product Code K508. Recalled by Apothecary Products, LLC. Units affected: 1,596 units.
Why was this product recalled? ▼
Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 21, 2023. Severity: Moderate. Recall number: Z-1703-2023.
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