Recall Z-1703-2023— Apothecary Products, LLC

Name: FDA recall Z-1703-2023
Creator: U.S. Food and Drug Administration
Published: 2023-03-30

Class II · Ongoing

Class II FDA medical device recall by Apothecary Products, LLC, initiated 2023-03-30. FDA's recall record names no specific 510(k) clearance for this event. Product: Medicine Dropper, Product Code K508. Reason: Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb..

Recalling firm: Apothecary Products, LLC
Classification: Class II
Status: Ongoing
Initiated: 2023-03-30
Firm location: Burnsville, MN, United States

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.