CooperVision recalls CLARITI 1 Day Toric Power -07.00 -1.25/010 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 axis mark is misaligned. This affects users who have this exact lens model and could lead to vision issues if not corrected.
The lens has an axis mark that may not align properly, causing the wearer to see blurry. This misalignment happens because the lens is designed for toric correction, which requires precise alignment to function correctly.
People who own or use the specific CooperVision CLARITI 1 Day Toric Power -07.00 -1.25/010 contact lens with UV blocker are affected. Those with this lens model are most at risk of experiencing blurred vision.
Check for the product name 'CLARITI 1 Day Toric Power -07.00 -1.25/010' and the lot number W0106186 on the packaging or lens box.
Look for the product name and lot number W0106186 on the packaging or lens box to confirm if it's recalled.
The recall states that misaligned axis marks can cause blurred vision, so it's recommended to check if you have the recalled model before using.
The recall does not specify a remedy, so you should check the packaging for the lot number and contact CooperVision for further guidance.
Check for the product name 'CLARITI 1 Day Toric Power -07.00 -1.25/010' and lot number W0106186 on the packaging or lens box.
We’ve drafted a message you can send CooperVision to request your refund or repair — edit it as you like.
Subject: Recall Z-2152-2021 — CooperVision CooperVision Hello, I own a CooperVision that is covered by recall Z-2152-2021 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.
