Alcon recalls Acrysof IQ IOLs with incorrect diopter settings that may cause vision issues. Affected models include 20.5 D SP ACRYLIC FOLDABLE LENS with UltraSert delivery system. Contact Alcon for details.
Incorrect IOL diopter
Alcon is recalling certain Acryso: IQ IOL lenses due to an incorrect diopter setting. This could lead to vision problems if the lens is implanted. Affected products have specific model numbers and lot codes.
The IOL (intraocular lens) has an incorrect diopter setting, which means it may not focus light properly on the retina. This could cause vision problems but does not pose a direct risk of injury.
People who have received the Acrysof IQ IOL with the incorrect diopter setting, particularly those who have had the lens implanted. The risk is low as the issue is related to the lens design rather than a safety hazard.
Check for model number AU00T0V205, lot number 12726594, or UDI # 038065GMN000065H7 on the product packaging. The product was sold with the UltraSert delivery system.
Look for model number AU00T0V205, lot number 12726594, or UDI # 038065GMN000065H7 on the product packaging.
The IOL has an incorrect diopter setting, which may cause vision problems.
If you have the affected IOL, contact Alcon for further instructions.
Check for model number AU00T0V205, lot number 12726594, or UDI # 038065GMN000065H7 on the product packaging.
We’ve drafted a message you can send Alcon to request your refund or repair — edit it as you like.
Subject: Recall Z-2287-2020 — Alcon Alcon Hello, I own a Alcon that is covered by recall Z-2287-2020 from Alcon. 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.
