CooperVision recalls AQUATE: 1 day toric contact lenses with UV blocker due to misaligned axis marks causing blurred vision. 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 because the axis mark can be misaligned, leading to blurred vision. This affects users who have the specific lot number mentioned in the recall.
The axis mark on the contact lens can become misaligned, which may cause blurred vision during use. This misalignment is a design issue that affects the lens's intended function for correcting vision.
Contact lens wearers who purchased the AQUATECH PLUS 1 DAY TORIC Power: -07.50 -0.75/060 model with lot number R0121629 are affected. People with vision correction needs are most at risk.
Check for the model name 'AQUATECH PLUS 1 DAY TORIC Power: -07.50 -0.75/060' and lot number R0121629 on the packaging or lens box.
Look for the model name and lot number R0121629 on the contact lens packaging or box.
The recall states that misaligned axis marks can cause blurred vision, so users should check if they have the affected lot number and follow the recall instructions.
Check the lot number on the packaging; if it matches R0121629, stop using it and contact CooperVision for further instructions.
The recalled lens has the model name 'AQUATECH PLUS 1 DAY TORIC Power: -07.50 -0.75/060' and lot number R0121629.
We’ve drafted a message you can send CooperVision to request your refund or repair — edit it as you like.
Subject: Recall Z-2144-2021 — CooperVision CooperVision Hello, I own a CooperVision that is covered by recall Z-2144-2021 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.
