CooperVision recalls FRESH DAY 1 DAY TORIC Power -07.50 -0. 75/060 daily disposable contact lenses with UV blocker due to potential blurred vision from misaligned axis marks.
Misaligned placement of an axis mark can cause the patient to experience blurred vision
CooperVision is recalling a specific type of daily disposable contact lens because it may cause blurred vision if the lens is not properly aligned. This recall affects users who have this exact lens model and could lead to vision issues if not addressed.
The lens has an axis mark that may not align correctly, causing the wearer to see blurry. This misalignment happens due to the lens design and can lead to vision problems if not properly fitted.
Contact lens wearers who have the specific FRESH DAY 1 DAY TORIC Power -07.50 -0.75/060 model with UV blocker are affected. Those with this lens model are most at risk of experiencing blurred vision.
Check for the model name 'FRESH DAY 1 DAY TORIC Power -07.50 -0.75/060' and the UV blocker feature on the lens packaging. This specific lens was sold with Lot Number R0121629.
Look for the model name 'FRESH DAY 1 DAY TORIC Power -07.50 -0.75/060' and UV blocker feature on the lens packaging.
The recall states that misaligned axis marks can cause blurred vision, so users should check if their lens is affected before continuing use.
Check the packaging for the model name 'FRESH DAY 1 DAY TORIC Power -07.50 -0.75/060' and UV blocker feature. This specific lens was sold with Lot Number R0121629.
The recall does not specify a remedy, so users should check the packaging to confirm if they have the affected model and contact CooperVision for further guidance.
We’ve drafted a message you can send CooperVision to request your refund or repair — edit it as you like.
Subject: Recall Z-2145-2021 — CooperVision CooperVision Hello, I own a CooperVision that is covered by recall Z-2145-2021 from CooperVision. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
