Bausch & Lomb recalls Akreos intraocular lenses (SKU AO60P0300) with a 16 diopter error instead of 3, risking vision impairment. Affected lenses have specific serial numbers and lot codes.
An off-power error was identified, which resulted in a diopter of 16, rather than the intended 3 diopter. Implantation of affected intraocular lens could result in functional visual impairment or reduction in visual acuity which could result in the need for optical or surgical correction.
Bausch & Lomb is recalling Akreos intraocular lenses with a 16 diopter error instead of the intended 3 diopter. This could cause vision problems requiring optical or surgical correction after implantation.
The lenses have a diopter error of 16 instead of 3, which can cause vision impairment. This error may lead to reduced visual acuity and the need for corrective measures like glasses or additional surgery.
People who received Akreos intraocular lenses with the specific serial numbers 1Q29212006 and 1Q29212010, or lot number 1Q29212, are affected. Patients who have had surgery with these lenses are most at risk.
Check for the serial numbers 1Q29212006 and 1Q29212010, or lot number 1Q29212 on the lens packaging. The product is sold under SKU AO60P0300.
Review the serial numbers and lot code on the lens packaging to confirm if it is affected.
The lenses have a diopter error of 16 instead of the intended 3, which could cause vision impairment or reduced visual acuity.
Check the serial numbers and lot code on the packaging to see if it is affected; contact Bausch & Lomb if unsure.
The recall record does not mention a remedy or fix.
We’ve drafted a message you can send Bausch & Lomb to request your refund or repair — edit it as you like.
Subject: Recall Z-2451-2025 — Bausch & Lomb Bausch & Lomb Hello, I own a Bausch & Lomb that is covered by recall Z-2451-2025 from Bausch & Lomb. 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.
