Systane Eye drops recalled due to fungal contamination

Systane eye drops recalled due to fungal contamination: FDA
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.
Alert: Alcon voluntarily recalls Systane Ultra PF lot due to potential fungal contamination
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.
Urgent Recall Issued for Alcon's Systane Eye Drops in Hawaii Over Potential Fungal Contamination Risks
Hawai‘i DOH warns against a contaminated lot of Systane Lubricant Eye Drops that could cause severe eye infections.
FDA Announces Nationwide Eye Drops Recall Due to Fungal Contamination
Systane eye drops were recalled earlier this week after the company discovered a fungal contamination in one of its products.
Recall: Systane eye drops may have possible 'fungal contamination' risk
The eye drops are typically used for temporary relief of burning and irritation for people with dry eye symptoms.
Eye drops recalled over fungal concerns: Here's which Systane products are impacted
Some Systane eye drops were recalled after a foreign material was found in a sealed container, according to an FDA recall announcement.
Systane eye drops recalled due to potential fungal contamination
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.
FDA announces recall of Systane eye drops due to fungal contamination
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.
Systane lubricant eye drops recalled for fungal contamination
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.
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