FDAJune 6, 2025device

Akreos, SKU: AO60P0300. Akreos intraocular lenses

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

bausch lomb surgicalbauschbausch lomb

UPCs

10757770501783

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →