Adverse reactions can be reported to the FDA's MedWatch program. In response to a report of foreign material found in a sealed vial, Alcon Laboratories has initiated a voluntary recall of Lot 10101 of ...

Fungal contamination of an eye product is known to potentially cause eye infections​​, which may be vision- or life-threatening, according to the FDA.

A single lot (Lot 10101) of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count, is being voluntarily recalled by Alcon Laboratories due to the detection of fungal material in a ...

Alcon Laboratories is voluntarily recalling one lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count (Lot 10101) to the consumer level. As of Dec. 23, Alcon Laboratories ...

The FDA announced Monday that Texas-based company Alcon Laboratories was voluntarily recalling one lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go following a consumer ...

“Alcon is conducting a voluntary recall of one (1) lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count (Lot 10101) distributed only in the United States following the ...

They are packaged in a green and pink cardboard box with the brand names Systane” and “ULTRA PF” printed on it, according to the FDA. The solution itself is in 25 plastic vials found in the box.

The recall impacts Systane Lubricant Eye Drops Ultra PF, Single Vials on-the-go 25 count boxes, lot # 10101 with an exportation date of September 2029, only. "Fungal contamination of an ophthalmic ...

On Dec. 21, Alcon Laboratories issued a voluntary recall of one lot of its Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25-count (Lot 10101) after a consumer complaint revealed ...

with “Systane” and “ULTRA PF” brand names on the front of the carton, and the “25 vials” package size marked Lot 10101 were recalled for possible fungal contamination on Dec.