Millions of prescription eye drop bottles have been recalled across the United States after federal regulators identified a potential contamination issue.
The Food and Drug Administration (FDA) recently classified a nationwide recall of more than 2.5 million bottles of Prednisolone Acetate Ophthalmic Suspension, USP, 1%, manufactured by Lupin Pharmaceuticals, as a Class II recall after the products were found to contain a potential foreign substance.
