CooperVision recalls Biofinity XR Toric Single Diagnostic soft contact lenses with misaligned axis causing incorrect power. Users may experience poor vision. Affected lot numbers: R24395839, R2440609: R24409954.
Manufactured with misaligned axis resulting in lenses with the incorrect power, users may experience poor visual acuity
CooperVision is recalling Biofinity XR Toric Single Diagnostic soft contact lenses that were manufactured with misaligned axis, which can cause incorrect power and poor visual acuity. This recall affects users who have the specific lot numbers listed in the notice.
The lenses were made with misaligned axis, leading to incorrect power. This can cause poor visual acuity for users who rely on the lenses for vision correction.
Contact lens wearers who purchased the Biofinity XR Toric Single Diagnostic soft lenses with the listed lot numbers are affected. People with vision correction needs are most at risk from incorrect lens power.
Check the lot numbers on your Biofinity XR Toric Single Diagnostic soft contact lenses: R24395839, R24406094, or R24409954. These specific lot numbers are affected by the recall.
Look for the lot numbers R24395839, R24406094, or R24409954 on your Biofinity XR Toric Single Diagnostic soft contact lenses.
The lenses were manufactured with misaligned axis, resulting in incorrect power which can cause poor visual acuity.
Check the lot numbers on your lenses; if they match the affected numbers, contact CooperVision for guidance.
Yes, users may experience poor visual acuity due to incorrect lens power from misaligned axis.
We’ve drafted a message you can send CooperVision to request your refund or repair — edit it as you like.
Subject: Recall Z-1198-2023 — CooperVision CooperVision Hello, I own a CooperVision that is covered by recall Z-1198-2023 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.
