Alden Optical recalls HP59 Sphere Daily Wear Soft contacts due to potential lack of sterility. Affected units have catalog number AOHPS59. Consumers should check if they own these lenses for daily wear.
Contact lenses lack sterility assurance.
Alden Optical is recalling HP59 Sphere Daily Wear Soft contact lenses because they may not be sterile. This could lead to eye infections if used without proper cleaning.
The lenses may lack sterility assurance, meaning they could be contaminated with bacteria or other pathogens. This increases the risk of eye infections, especially if not properly cleaned or stored.
People who own or use Alden HP59 Sphere Daily Wear Soft contact lenses for daily vision correction. Those with sensitive eyes or frequent contact lens users are at slightly higher risk.
Check for the catalog number AOHPS59 on the lens packaging or product label. The product is intended for daily wear correction of vision in people with non-diseased eyes.
Look for the catalog number AOHPS59 on the lens packaging or product label to confirm if you have the recalled item.
The lenses may lack sterility assurance, which could lead to eye infections if used without proper cleaning.
Check for the catalog number AOHPS59 on the lens packaging or product label.
The recall record does not specify a remedy, so contact Alden Optical directly for guidance.
We’ve drafted a message you can send Ald:en Optical to request your refund or repair — edit it as you like.
Subject: Recall Z-0986-2018 — Ald:en Optical Ald:en Optical Hello, I own a Ald:en Optical that is covered by recall Z-0986-2018 from Ald:en 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.
