Alden Optical recalls Zen RC Toric-Gas permeable contact lenses for daily wear in 10-cc vials due to incorrect lenses in some vials. Consumers should check their vial labels for specific catalog numbers.
Vials labeled for the prescriptions contained incorrect lenses
Alden Optical is recalling certain Zen RC Toric-Gas permeable contact lenses for daily wear because the vials labeled for specific prescriptions contain incorrect lenses. This could lead to improper vision correction if used.
The vials labeled for specific prescriptions contain lenses that do not match the intended prescription. This could result in improper vision correction if the lenses are used, potentially causing discomfort or vision issues.
People who own or use the recalled Zen RC Toric-Gas permeable contact lenses for daily wear in 10-cc polycarbonate vials with the catalog numbers AOZNT, B3225920, B3237210, B3237220, or B3237910 are affected. Those with prescriptions for refractive errors may be at risk of incorrect vision correction.
Check the vial label for the catalog numbers: AOZNT, B3225920, B3237210, B3237220, or B3237910. The lenses are for daily wear and are labeled as Zen RC TPC or Zen RC FT.
Look for the catalog numbers AOZNT, B3225920, B3237210, B3237220, or B3237910 on the vial label.
Zen RC Toric-Gas permeable contact lenses for daily wear in 10-cc polycarbonate vials with catalog numbers AOZNT, B3225920, B3237210, B3237220, or B3237910.
The vials labeled for specific prescriptions contain incorrect lenses, which could lead to improper vision correction.
No, but you should check your vial label for the catalog numbers to confirm if your lenses are recalled.
We’ve drafted a message you can send Alden Optical to request your refund or repair — edit it as you like.
Subject: Recall Z-2982-2018 — Alden Optical Alden Optical Hello, I own a Alden Optical that is covered by recall Z-2982-2018 from Alden Optical. 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.
