CooperVision recalls limited lots of MyDay Toric contact lenses for astigmatism due to incorrect cylinder power. Consumers should check lot numbers and contact CooperVision for a replacement.
a limited number of lots were manufactured with an incorrect cylinder power.
CooperVision is recalling specific lots of MyDay Toric contact lenses for astigmatism because some were made with the wrong cylinder power. This could lead to improper vision correction and discomfort or eye damage if worn.
The lenses were manufactured with an incorrect cylinder power, which means they may not correct astigmatism properly. This can cause blurred vision, eye strain, or discomfort when worn.
Contact lens wearers who purchased the recalled MyDay Toric, LensCrafters One Day Premium Daily Disposable, or similar brands with the listed lot numbers are affected. People with astigmatism who use these lenses daily are most at risk.
Check the blister pack lot numbers: 6461501582, 6461501590, 6448502235, or 6472500679. Also look for carton lot numbers listed in the record.
Look for blister pack lot numbers: 6461501582, 6461501590, 6448502235, or 6472500679.
Reach out to CooperVision for a replacement or refund if you have the recalled lot numbers.
CooperVision found that a limited number of lots were manufactured with an incorrect cylinder power, which could lead to improper vision correction.
Check the blister pack lot numbers: 6461501582, 6461501590, 6448502235, or 6472500679. Also look for carton lot numbers listed in the record.
No, but you should check your lot numbers and contact CooperVision for a replacement if you have the recalled items.
We’ve drafted a message you can send CooperVision to request your refund or repair — edit it as you like.
Subject: Recall Z-1455-2025 — CooperVision CooperVision Hello, I own a CooperVision that is covered by recall Z-1455-2025 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.
