One lot of Systane Lubricant Eye Drops Ultra PF, manufactured by Alcon Laboratories, has been recalled due to fungal contamination, the FDA announced this week.

In response to a report of foreign material found in a sealed vial, Alcon Laboratories has initiated a voluntary recall of Lot 10101 of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count.

Hawai‘i DOH warns against a contaminated lot of Systane Lubricant Eye Drops that could cause severe eye infections.

Systane eye drops were recalled earlier this week after the company discovered a fungal contamination in one of its products.

The recall affects one lot of Systane Lubricant Eye Drops Ultra PF, sold in a 25-count box of single vials, which are used to temporarily relieve eye burning and irritation, the FDA said.

The FDA has issued a recall for specific lots of Systane eye drops due to potential fungal contamination after a consumer complaint. Users are advised to stop using the product immediately and return it for a refund or replacement.

The recalled Systane Lubricant Eye Drops Ultra PF were sold as single-use plastic vials in 25-packs, according to the recall notice posted by the Food and Drug Administration. They’re marked with the lot number 10101 and a September 2025 expiration date.