Clerio Vision recalls specific contact lens lots (UPC 675506803334 and 675506804478) due to incorrect lens power. These lenses may cause vision issues if used.
One lot of contact lenses labeled as BC MED, DIA 14.0 PWR -2.25 contained BC MED, DIA 14.0, PWR -3.75 contact lenses
Clerio Vision is recalling two specific lots of contact lenses that contain the wrong power (PWR -3.75 instead of -2.25). Using these lenses could lead to vision problems because they are not designed for the intended correction.
The recalled lenses have a power of -3.75 diopters instead of the labeled -2.25 diopters. This mismatch could cause vision issues for users who need precise correction, especially those with specific prescription requirements.
People who own the recalled contact lens lots (UPC 675506803334 or 675506804478) and wear them for daily vision correction. Those with higher prescription needs may be at slightly greater risk.
Check the UPC codes on the packaging: 675506803334 (6 lenses) or 675506804478 (12 lenses). The lot number 3100246509 and expiration date 2026/09 are also associated with this recall.
Look for the UPC codes 675506803334 (6 count) or 675506804478 (12 count) on the packaging.
The recall indicates the lenses have the wrong power (-3.75 instead of -2.25), which could cause vision issues. They are not safe for use as intended.
Check the UPC codes on the packaging to see if you have the recalled lots. If you do, contact Clerio Vision for further instructions.
The recalled lenses have UPC 675506803334 (6 count) or 675506804478 (12 count) with lot number 3100246509 and expiration date 2026/09.
We’ve drafted a message you can send Clerio Vision to request your refund or repair — edit it as you like.
Subject: Recall Z-0808-2021 — Clerio Vision Clerio Vision Hello, I own a Clerio Vision that is covered by recall Z-0808-2021 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.
