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If you have the recalled Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count (Lot 10101) stop using them immediately. Return the eye drops to the place of purchase for a ...
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.
Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count: Lot 10101, which expires in September 2025. The eye ...
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.
Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count: Lot 10101, which expires in September 2025. The eye drops are used to temporarily relieve "burning and irritation in persons ...
RECALL: Systane Lubricant Eye Drops Ultra PF in 25-count packages with the lot number 10101, which are set to expire in September 2025. The recalled products were sold at Publix .
The eye drops recalled, used to treat symptoms of dry eye, were sold in 25-count on-the-go single vials with lot number 10101 and an expiration date of September 2025.
One lot of Systane Lubricant Eye Drops Ultra PF was recalled following a consumer complaint “of foreign material observed inside a sealed single-use vial." IE 11 is not supported.
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.
Systane brand eye drops were voluntarily recalled because of possible fungal contamination, the Food and Drug Administration said. One lot of Systane Lubricant Eye Drops Ultra PF was recalled ...
A popular brand of eye drops is being recalled nationwide because of possible contamination. Alcon Laboratories in Texas is voluntarily recalling Systane Lubricant Eye Drops Ultra P-F following a ...
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 ...
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