FDA Recalls Millions of Prednisolone Acetate Eye Drop Bottles Due to Contamination Risk

The U.S. Food and Drug Administration has issued a Class II nationwide recall for more than 2.5 million bottles of prednisolone acetate ophthalmic suspension eye drops. Manufactured by Lupin Limited, the prescription eye drops are being recalled due to the potential presence of foreign particulate matter. This contamination could cause adverse reactions such as inflammation, irritation, and damage to the cornea.