Alden Optical recalls Zenlens Toric-Gas Permeable Contact Lenses for Daily Wear in 10-cc vials due to incorrect lenses in some prescription vials. Affected vials have specific lot numbers and UDI codes.
Vials labeled for the prescriptions contained incorrect lenses
Alden Optical is recalling certain Zenlens 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 incorrect lenses, which could result in improper vision correction if used. This is a labeling issue rather than a physical defect in the lenses themselves.
People who own or use the recalled Zenlens Toric-Gas Permeable Contact Lenses for Daily Wear in 10-cc polycarbonate vials with the listed lot numbers and UDI codes are affected. Those with prescriptions for these lenses are most at risk.
Check for vials labeled 'Zenlens FT', 'Zenlens Toric-Zenlens FT + MV', 'Zenlens TPC', or 'Zenlens TPC + FT' with the catalog number AOZNT. Look for specific lot numbers and UDI codes listed in the recall notice.
Look for the catalog number AOZNT and specific lot numbers or UDI codes listed in the recall notice.
The vials labeled for specific prescriptions contain incorrect lenses, which could lead to improper vision correction if used.
Check the vial label for the catalog number AOZNT and specific lot numbers or UDI codes listed in the recall notice. If they match, stop using them and contact Alden Optical.
The recall is due to incorrect lenses in some vials, which could cause improper vision correction. There is no risk of injury or damage to the eyes from using these lenses.
We’ve drafted a message you can send Alden Optical to request your refund or repair — edit it as you like.
Subject: Recall Z-2981-2018 — Alden Optical Alden Optical Hello, I own a Alden Optical that is covered by recall Z-2981-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
