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The recalled products were sold at Publix, the chain said in a recall notice dated Dec. 20. What could happen if the eye drops are used? The recalled eye drops could cause an eye infection ...
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 ...
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 ...
FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.
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One lot of eye drops is being voluntarily recalled due to potential fungal contamination, the U.S. Food and Drug Administration announced earlier this week. The eye drops, Systane Lubricant Eye ...
Eye drops are being recalled due to a rare bacterium found in artificial tears. Find a list of recalled drops in 2023. Plus, eye infection symptoms.
The recall involves Samurai-branded white-and-silver plastic mini smoke alarms, model number SM1, which is indicated on the packaging. Recalled Samurai Mini Smoke Alarm — front / Credit: U.S ...