CooperVision recalls SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lenses with UV blocker due to potential blurred vision from misaligned axis marks. Affected lenses have Lot Number U0108940.
Misaligned placement of an axis mark can cause the patient to experience blurred vision
CooperVision is recalling a specific type of daily disposable contact lens that may cause blurred vision if the axis mark is misaligned. This issue could affect users who rely on precise lens alignment for clear vision.
The contact lens has an axis mark that may be misaligned, causing blurred vision. This misalignment happens because the lens is designed for specific rotational positioning, and improper alignment affects vision clarity.
People who own or use the SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lenses with UV blocker (Lot Number U0108940) are affected. Those with specific vision needs who require precise lens alignment are most at risk.
Check for the product name 'SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker' and Lot Number U0108940 on the packaging or lens box.
Look for the Lot Number U0108940 on the lens packaging or box to confirm if it's affected.
The recall indicates a potential risk of blurred vision due to misaligned axis marks, but the lenses are generally safe if properly aligned.
Check for the Lot Number U0108940 on the packaging or lens box. Affected lenses have this specific lot number.
The recall does not require stopping use; however, you should check the lot number to confirm if your lenses are affected.
We’ve drafted a message you can send CooperVision to request your refund or repair — edit it as you like.
Subject: Recall Z-2148-2021 — CooperVision CooperVision Hello, I own a CooperVision that is covered by recall Z-2148-2021 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.
