The recall was initiated on April 23, but the Food and Drug Administration listed it as a Class II on May 6, according to agency documentation. In all, 75,795 cases have been recalled, or 1.8 million ...

An eye drop manufacturer has announced a voluntary recall of certain dry eye drops after an audit from the U.S. Food and Drug Administration found "manufacturing cGMP deviations," and has advised that ...

Some lots of a globally distributed eye drops may not fulfill the promise of its name. Two lots of Purely Soothing eye drops sold by online retailers and at trade shows have been recalled by ...

The pharmaceutical retailer AvKARE has published a voluntary recall notice for five different types of eye drops previously available through the company’s online store. The recall involves products ...

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 ...

Several eye care products have been recalled nationwide due to potential safety risks. BRS Analytical Service, LLC initiated the voluntary recall after manufacturing issues raised possible concerns ...

Systane Lubricant Eye Drops in a green and pink carton design, with “Systane” and “ULTRA PF” brand names on the front of the carton, and the “25 vials” package size marked Lot 10101 were recalled for ...

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 ...