CooperVision recalls Biofinity Toric Multifocal Contact Lenses with specific lot numbers due to potential incomplete seals that could render lenses unsterile. Consumers should check their carton lot numbers and contact CooperVision for details.
Lens blisters may have an incomplete or leaking seal which may render them unsterile.
CooperVision is recalling Biofinity Toric Multifocal Contact Lenses with certain lot numbers because the lenses might have seals that don't close properly, making them unsterile. This could lead to eye infections if used.
The lenses may have an incomplete or leaking seal, which can compromise sterility. If the seal fails, the lenses might become contaminated and cause eye infections when worn.
Contact lens wearers who purchased Biofinity Toric Multifocal Lenses with the listed carton lot numbers. People with sensitive eyes or those who use lenses frequently are at slightly higher risk.
Check the carton for lot numbers starting with RB0684 or RC1759. The specific lot numbers are listed in the recall notice. This product was sold in the U.S. and Canada.
Look for the lot number on the carton of your Biofinity Toric Multifocal Contact Lenses. The recall includes specific lot numbers listed in the notice.
The recall does not require immediate discontinuation. However, if your lot number is listed, you should check with CooperVision for instructions.
Contact CooperVision directly to get specific instructions for your lenses. They may provide a replacement or refund.
If the seal is incomplete, the lenses could become unsterile and cause eye infections. However, the risk is low and depends on the specific lot number.
We’ve drafted a message you can send CooperVision to request your refund or repair — edit it as you like.
Subject: Recall Z-2166-2025 — CooperVision CooperVision Hello, I own a CooperVision that is covered by recall Z-2166-2025 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.
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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.
