CooperVision Recalls Pearle Vision 1 Day Contact Lenses Due to Incorrect Power

CooperVision Inc. initiated a Class II recall for Pearle Vision 1 day (somofilcon A) contact lenses after discovering that a small number of lenses in one lot had the incorrect power. The US Food and Drug Administration announced the recall, listing the affected product quantity as 3,060 units. The recall began on August 12 and was classified as Class II by the FDA on September 18. The specific affected product is identified by Carton Lot # 11727620152030 and Blister Lot # CB132348, with distribution limited to Minnesota, Ohio, and Wisconsin.