Eye Drops Recalled Due to Fungal Contamination, Potential Eye Infection Risk

The Food and Drug Administration (FDA) has issued a recall on certain eye drops due to potential fungus contamination. Alcon Laboratories, the makers of Systane, voluntarily recalled one lot of their Systane Lubricant Eye Drops Ultra PF after a customer reported finding “foreign material” in the drops, which was later determined to be fungal in nature.

While no health issues have been reported in connection with the recalled eye drops, fungal contamination can lead to serious eye infections, especially in individuals with compromised immune systems. The recalled product, Systane Lubricant Eye Drops Ultra PF Single Vials On-the-Go, 25 count with lot number 10101 and expiration date of September 2025, was distributed nationwide at various retailers.

The FDA is advising consumers to stop using the recalled eye drops immediately and return them to the place of purchase for a refund or replacement. Individuals who have used the eye drops and experience any health issues should contact their healthcare provider and report the problem to the FDA’s MedWatch Adverse Event Reporting program.

Symptoms of a fungal eye infection can manifest days to weeks after exposure and may include redness, pain, sensitivity to light, blurred vision, and discharge. Certain groups, such as those with diabetes, weakened immune systems, or who use corticosteroids, are at a higher risk of developing a fungal eye infection.

If you have used the recalled eye drops and are experiencing symptoms, contact your healthcare provider for diagnosis and treatment. Stay informed and take necessary precautions to protect your eye health.