Z-1703-2023 Class II Ongoing
FDA device recall Z-1703-2023 was initiated by Apothecary Products, LLC on March 30, 2023 and is designated Class II. Reason for recall: Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb. The recall status is ongoing. Affected quantity: 1,596 units.
Recall Details
- Product Type
- Devices
- Report Date
- June 21, 2023
- Initiation Date
- March 30, 2023
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,596 units
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.
Distribution Pattern
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.
Code Information
Lot Number: 021623; UPC Number: 077602005085