Millions of bottles of prescription eye drops have been recalled nationwide. Here are the affected items and the reasoning behind the recall.

The FDA said it was a Class II recall, meaning that using the drops may raise the risk of suffering temporary damage to the eyes or vision.

The Food and Drug Administration has recalled nearly 12 million Rohto eye drop products nationwide after determining the manufacturer could not assure the products were sterile.

Millions of bottles of popular over-the-counter eye drops used to treat redness, dryness and eye strain have been recalled due to concerns about their sterility.

More than 12 million bottles of over-the-counter eye drops sold nationwide — including in Pennsylvania — have been recalled. Rohto-brand eye drops were recalled under a class II FDA categorization, ...

Millions of eye drops from the brand Rohto have been recalled due to a potential lack of sterility. Here's how to identify affected products.

Nearly 12 million bottles of Rohto Cooling Eye Drops face a Class II recall over lack of assurance of sterility, affecting eight product lines.

NEW YORK (WPIX) – Millions of bottles of eye drop medication widely used to treat allergies and inflammation have been recalled across the country, according to the Food and Drug Administration.

Lupin Pharmaceuticals is voluntarily recalling more than 2.5 million bottles of Prednisolone Acetate Ophthalmic Suspension eye drops due to a possible foreign substance found in the product.

The eye drops could cause adverse health effects if used, according to the FDA.

Here’s what you need to know.