Lupin Pharmaceuticals Recalls 2.5 Million Bottles of Prescription Eye Drops
By Kelly Cloonan
Lupin Pharmaceuticals voluntarily recalled more than 2.5 million bottles of prescription eye drops it manufactured, according to the Food and Drug Administration.
The FDA said Lupin initiated the recall on June 4, citing the potential presence of a foreign substance.
The recall is for certain bottles of prednisoloneacetate ophthalmic suspension eye drops, which are used to eye allergies and inflammation.
Write to Kelly Cloonan at kelly.cloonan@wsj.com
(END) Dow Jones Newswires
July 09, 2026 18:44 ET (22:44 GMT)
Copyright (c) 2026 Dow Jones & Company, Inc.The articles, information, and content displayed on this webpage may include materials prepared and provided by third parties. Such third-party content is offered for informational purposes only and is not endorsed, reviewed, or verified by Morningstar.
Morningstar makes no representations or warranties regarding the accuracy, completeness, timeliness, or reliability of any third-party content displayed on this site. The views and opinions expressed in third-party content are those of the respective authors and do not necessarily reflect the views of Morningstar, its affiliates, or employees.
Morningstar is not responsible for any errors, omissions, or delays in this content, nor for any actions taken in reliance thereon. Users are advised to exercise their own judgment and seek independent financial advice before making any decisions based on such content. The third-party providers of this content are not affiliated with Morningstar, and their inclusion on this site does not imply any form of partnership, agency, or endorsement.
Popular
The 10 Best Companies to Invest in Now
14 Elite Funds and ETFs, and 5 Popular Funds That Just Missed the Mark
3 Stocks to Sell and 3 Stocks to Buy for October
The Top Funds for a Simpler Retirement Portfolio
