The affected packages of Systane Lubricant Eye Drops Ultra PF Single Vials On-the-Go were recalled after a customer complaint of "foreign material observed inside a sealed single use vial," the ...

The FDA published the recall of Systane eye drops during Christmas Week, warning the public of a possibly dangerous fungal infection. The recall impacts Systane Lubricant Eye Drops Ultra PF, Single ...

There is no shortage of products to turn to this holiday season if you're suffering from dry eyes, but there is one brand you shouldn't purchase nor use for the time being. Here's what you need to ...

The eye drops, Systane Lubricant Eye Drops Ultra PF, are single vial drops available in a 25-count box and manufactured by Alcon Laboratories, based in Fort Worth, Texas. "Alcon evaluated a ...

Fort Worth, Texas-based Alcon Laboratories has voluntarily recalled one lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, which are packaged in batches of 25.

Alcon Laboratories voluntarily recalled a single lot of Systane Lubricant Eye Drops Ultra PF after it ... that people can do one of the following: Complete and submit a report online Download ...

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 ...

Select eye drops under the Systane brand were voluntarily recalled for concerns of fungal contamination, which could cause eye infection and threaten users' vision, according to a recall ...

Alcon Laboratories in Fort Worth, Texas recalled one lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count on December 21. The recall impacts Lot 10101 with an expiration ...

Select eye drops under the Systane brand were voluntarily recalled for concerns of fungal contamination, which could cause eye infection and threaten users' vision, according to a recall announcement ...

Some Systane eye drops were recalled after a foreign material was found in a sealed container, according to an FDA recall announcement.