Clerio Vision recalls Extreme H2O 59% contact lenses that may be mislabeled with incorrect lens power. Affected lenses have specific lot numbers and UPC codes. Consumers should check their lenses for proper labeling.
Contact lenses may be mislabeled with the incorrect lens power.
Clerio Vision is recalling Extreme H2O 59% spherical soft contact lenses for daily wear because they may be mislabeled with the wrong lens power. This could lead to improper vision correction if the lenses are used without the correct prescription.
The lenses may have incorrect lens power labels, which could result in improper vision correction. This might cause blurry vision or discomfort if the lenses are not the right prescription for the user's eyes.
People who own or use Extreme H2O 59% contact lenses with lot number 0114511565 or UPC codes 675506700657 (6-pack) or 675506668650 (individual) are affected. Those with astigmatism under 0.75 Diopters may be at higher risk if the lenses are mislabeled.
Check for lot number 0114511565 or UPC codes 675506700657 (6-pack) or 675506668650 (individual) on the packaging. The lenses are intended for daily wear and correction of vision in people with non-diseased eyes.
Look for the lot number 0114511565 or UPC codes 675506700657 (6-pack) or 675506668650 (individual) on the lens packaging.
The lenses may be mislabeled with the incorrect lens power, which could lead to improper vision correction.
Check the lot number or UPC codes on the packaging to see if your lenses are affected. If they are, contact Clerio Vision for further instructions.
Yes, mislabeled lenses could cause blurry vision or discomfort if they are not the correct prescription for your eyes.
We’ve drafted a message you can send Clerio Vision to request your refund or repair — edit it as you like.
Subject: Recall Z-1352-2021 — Clerio Vision Clerio Vision Hello, I own a Clerio Vision that is covered by recall Z-1352-2021 from Clerio Vision. 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.
