CooperVision recalls Biofinity Toric Multifocal Soft Contact Lenses with misaligned axis causing incorrect power. This may lead to poor visual acuity. Check lot numbers listed for affected products.
Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity
CooperVision is recalling Biofinity Toric Multifocal Soft Contact Lenses that were manufactured with a misaligned axis, resulting in lenses with incorrect power. This could cause poor visual acuity for users. The recall affects specific lot numbers.
The lenses were manufactured with a misaligned axis, which means they have the incorrect power for correcting vision. This can lead to poor visual acuity, especially for people who need correction for myopia, hyperopia, and astigmatism with presbyopia.
People who own or use the recalled Biofinity Toric Multifocal Soft Contact Lenses with the listed lot numbers. Those with presbyopia and astigmatism are most at risk due to the lens correction issues.
Check the lot numbers listed in the recall: RB0444532, RB0450357, and other specific numbers provided in the record. These lot numbers correspond to the affected Biofinity Toric Multifocal Soft Contact Lenses.
Verify your lenses' lot numbers against the list provided in the recall to determine if they are affected.
The lenses were manufactured with a misaligned axis, resulting in incorrect power which may cause poor visual acuity.
Check your lot numbers against the list provided in the recall. If affected, you may need to contact CooperVision for further instructions.
Yes, individuals with presbyopia and astigmatism are most at risk due to the lens correction issues.
We’ve drafted a message you can send CooperVision to request your refund or repair — edit it as you like.
Subject: Recall Z-3311-2024 — CooperVision CooperVision Hello, I own a CooperVision that is covered by recall Z-3311-2024 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.
