The US Food and Drug Administration (FDA) announced a Class II recall for Pearle Vision 1 day (somofilcon A) contact lenses. CooperVision Inc. initiated the ongoing recall due to a small number of lenses within the affected lot that are of the incorrect power. The FDA lists the product quantity as 3,060.

The recall was initiated on August 12 and classified as Class II by the FDA on September 18. The affected product was distributed in Minnesota, Ohio, and Wisconsin, according to the FDA.

The recall number is Z-3248-2026. The affected product is identified by Carton Lot # 11727620152030 and Blister Lot # CB132348.