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FDA Recalls 2.5M Eye Drop Bottles | Dover News
Description
FDA just recalled over 2.5 million bottles of prescription eye drops—Prednisolone Acetate Ophthalmic Suspension—due to possible contamination that could cause temporary health issues. The recall, upgraded to Class Two in June, affects 1% strength bottles in 5, 10, and 15 mL sizes. If you’ve been prescribed these, check your lot number and stop using them immediately. Dispose safely and consult your doctor or pharmacist for a replacement. Your eyes are too important to risk.
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