CooperVision recalls CLARITI 1 Day Toric contact lenses with UV blocker due to potential blurred vision from misaligned axis marks. Affected lot R0121629.
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 that may cause blurred vision if the axis mark is misaligned. This could affect users who have the lens model with lot number R0121629.
The lens has an axis mark that can become misaligned, leading to blurred vision. This misalignment might happen during insertion or use, but it doesn't cause injury or damage.
People who own or use the CLAR: 1 Day Toric contact lens with lot number R0121629 are affected. Those with the specific lens model and UV blocker are most at risk.
Check for the lens model: CLARITI 1 Day Toric Power: -07.50 -0.75/060 with UV blocker. The affected lot number is R0121629.
Identify if your lens is the CLARITI 1 Day Toric Power: -07.50 -0.75/060 with UV blocker.
The recall states it may cause blurred vision due to misaligned axis marks, but it does not cause injury or damage.
Check if your lens matches the model and lot number described in the recall. If it does, contact CooperVision for guidance.
The affected lot number is R0121629. Check the packaging for this specific lot number.
We’ve drafted a message you can send CooperVision to request your refund or repair — edit it as you like.
Subject: Recall Z-2143-2021 — CooperVision CooperVision Hello, I own a CooperVision that is covered by recall Z-2143-2021 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.
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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.
