[ad_1]
-
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 fungal contamination after a consumer reported a foreign object floating in a vial.
-
At the time of publication, there have been no adverse reactions reported.
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 Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count (Lot 10101) due to a customer complaint about a foreign object in a vial that the company says was fungal contamination.
The single lot of Systane Lubricant Ultra PF eye drops are the only drops from the brand affected by the recall. Aside from the customer complaint, there have been no adverse reactions reported, the recall said, however, the call was made out an “abundance of caution,“ an Alcon spokesperson told People, because fungal contamination in eye products can cause eye infections. Those infections can be vision-threatening, and in very rare cases potentially life-threatening in immunocompromised patients, the FDA added.
This recall comes after a string of contamination-related eye drop recalls rolled out last year.
Systane Lubricant Ultra PF eye drops are meant for the temporary relief of burning and irritation caused by dry eye. The package is made of green cardboard and contains 25 sterile, single-use plastic vials with the identification number NDC 0065-1432-06 or UPC 300651432060. The only lot affected is number 10101 which expires in September 2025.
An Alcon spokesperson said that investigation of the contamination is still ongoing, however, the foreign material report appears to be an isolated incident.
If you purchased the recalled product, the FDA and Alcon urge you to stop using the drops immediately and return them to your place of purchase for a replacement or refund. If you have questions regarding the recall, you can contact Alcon Laboratories at 1-800-241-5999 between 7:30 a.m. and 6:00 p.m. CST between Monday and Friday. If you have concerns regarding a potential reaction to the product, you should contact your doctor.
To report a potential reaction to the FDA, you can submit a form online with the MedWatch Adverse Event Reporting program.
You Might Also Like
[ad_2]
Source link