FDA Announces Recall of Nearly 750,000 Bottles of Eye Drops Due to Sterility Concerns

The U.S. Food and Drug Administration (FDA) has designated a Class II recall for nearly 750,000 bottles of various eye care products, including lubricant eye drops, a hypertonicity eye solution, and a nighttime eye ointment, due to a lack of assurance of sterility. The recall was initiated by Sterling Pharmaceutical Services LLC.