Nationwide Recall: Eye Drops Pulled Over Fungal Contamination Risk

United States -Consumers are being urged to check their medicine cabinets as a brand of eye drops sold across the United States has been recalled due to potential fungal contamination, which could lead to vision damage.

The Food and Drug Administration (FDA) announced Monday that Alcon Laboratories, a Texas-based company, is voluntarily recalling a single lot of its “Systane Lubricant Eye Drops Ultra SPF, Single Vials On-the-Go” product. The recall involves 25-count packages of the eye drops, which may contain fungal contamination.

What Prompted the Recall?

The recall was initiated after a consumer reported finding a “foreign material” in a sealed vial of the eye drops. Upon investigation, Alcon Laboratories confirmed the material was fungal in nature.

This recall adds to a growing list of eye drop contamination issues reported in recent years, with dozens of products pulled from shelves in 2023 due to similar concerns.

Potential Risks of Fungal Contamination

Fungal contamination in eye care products can cause infections that threaten vision. While such infections are typically treatable, they can become severe and even life-threatening for immunocompromised individuals.

Alcon Laboratories stated that, to date, there have been no reported infections linked to the recalled eye drops.

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How to Identify the Recalled Product

If you have purchased Systane-brand eye drops, you can check if your product is affected by locating the following details on the packaging:

  • Lot Number: 10101
  • UPC: 300651432060
  • NDC: 0065-1432-06
  • Expiration Date: September 2025

The affected product was distributed nationwide through retail stores and online platforms.

What to Do If You Have the Recalled Product

Consumers who have the recalled eye drops should stop using them immediately and follow the FDA’s guidance for returns or disposal.

If you experience any adverse effects after using the product, you are encouraged to report your case to the FDA through the MedWatch Adverse Event Reporting Program here.

Final Note

This recall serves as a reminder to stay vigilant about product safety and regularly check for updates from the FDA regarding consumer products. For more information or assistance, visit the FDA’s official website.

Alton Walker

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