The Food and Drug Administration issued a nationwide recall of single-use eyedrops. One lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count (Lot 10101) was recalled over ...

However, out of an abundance of caution, Alcon has initiated a voluntary recall and notified the US FDA." Eye Drop Recall Recommended by FDA After 27 Popular Brands Flagged for Possibly Causing ...

The product may be used to treat a condition that the American Academy of Ophthalmology says affects around 20 million ...

One lot of Systane Lubricant Eye ... the FDA’s MedWatch Adverse Event Reporting program online, by regular mail, or by fax. Fungal eye infections are very rare but can be serious. The recall ...

Select eye drops under the Systane brand were ... material in a sealed single-use vial of the eye drop solution, according to the recall announcement. The company determined the material was ...

MORE: Be wary of unproven eye drop treatment with amniotic fluid, FDA says "Alcon is conducting a voluntary recall of one (1) lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go ...

The Food and Drug Administration issued a nationwide recall of single-use eyedrops. One lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count (Lot 10101) was recalled over ...

The Food and Drug Administration (FDA) announced a nationwide recall of a popular single-use eye drop on December 23. Alcon Laboratories, maker of Systane eyedrops, voluntarily recalled one lot of ...