The FDA has announced a recall of specific eye drops over concerns about possible fungus contamination. Alcon Laboratories has voluntarily pulled back one lot of its Systane Lubricant Eye Drops Ultra PF after a customer reported finding “foreign material” in the product. Upon investigation, Alcon discovered that the material was fungal.
Fungal contamination in eye drops can lead to eye infections, which could seriously threaten vision and potentially be life-threatening for individuals with weakened immune systems. Thankfully, no health issues related to the recalled eye drops have been reported so far.
The recall concerns Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, in a 25-count pack. This lot has the number 10101 and expires in September 2025. These drops were sold nationwide through online retailers and in stores like Target, Kroger, Walmart, and Walgreens.
The FDA advises anyone with this product to stop using it immediately and return it for a refund or replacement. If any health problems potentially connected to the use of these eye drops occur, consumers should reach out to their healthcare providers and report it to the FDA’s MedWatch Adverse Event Reporting program online, by mail, or fax.
Though fungal eye infections are rare, they can be severe. The recall notice did not specify the type of fungus found in the Systane eye drops, but various fungi can cause infections if they come into contact with the eyes or reach the eyes through the bloodstream.
Symptoms of a fungal eye infection can emerge several days to weeks after exposure, and can include eye problems. People at heightened risk for these infections include those with diabetes, compromised immune systems, or who are taking corticosteroids. If you experience signs of infection after using the recalled drops, consult your healthcare provider as treatment will differ based on the diagnosis.
