CooperVision recalls BIOFINITY XR TORIC soft contact lenses with misaligned axes that may cause poor visual acuity. Affected lot numbers listed. Consumers should contact CooperVision for details.
Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity
CooperVision is recalling certain BIOFINITY XR TORIC soft contact lenses that have a misaligned axis, which can lead to poor vision. This recall affects specific lot numbers and may cause vision issues if the lenses are used without correction.
The lenses were manufactured with a misaligned axis, meaning they have the incorrect power for vision correction. This can result in poor visual acuity, especially for people who need precise correction for conditions like astigmatism or presbyopia.
People who own or use the recalled BIOFINITY XR TORIC soft contact lenses with the listed lot numbers. Those with astigmatism or presbyopia may be most affected due to the lenses' intended use.
Check the lot numbers listed in the recall: RD0122830, RD0122954, and other specific codes provided in the official notice. These lenses are sold by CooperVision for correcting vision issues including astigmatism.
Verify if your lenses have the specific lot numbers listed in the recall notice.
No, the recall states the lenses may cause poor visual acuity but does not mention serious injury risks.
Check the lot numbers on your lens packaging against the list provided in the recall notice.
Contact CooperVision directly for further instructions on how to handle the lenses.
We’ve drafted a message you can send CooperVision to request your refund or repair — edit it as you like.
Subject: Recall Z-3310-2024 — CooperVision CooperVision Hello, I own a CooperVision that is covered by recall Z-3310-2024 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.
