FDA recalls millions of Lupin eye drops over possible contaminant
The FDA has recalled more than 2.5 million bottles of Lupin's prednisolone acetate eye drops due to a possible foreign substance; the substance and its entry method aren’t identified. The affected bottles (5 mL, 10 mL, 15 mL) are from India-based Lupin and are used to reduce inflammation after eye surgery or for allergies. Because this is a Class II recall (high risk), patients should not stop using the product on their own and should consult an eye doctor or pharmacist for guidance based on their condition.
