FDA recall record

Bausch & Lomb Surgical Akreos, SKU: AO60P0300 recall — FDA Z-2451-2025

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…

Class IIIclassification
Z-2451-2025official record ID
Sep 3, 2025report date

Recall record at a glance

Official recordZ-2451-2025
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusOngoing
Recalling firmBausch & Lomb Surgical, Inc.
Report dateSep 3, 2025
Recall initiation dateJun 6, 2025
Quantity2
LocationClearwater, FL, United States

Official product description

Akreos, SKU: AO60P0300. Akreos intraocular lenses

Why the product was recalled

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.

Distribution information

US: AZ, CA

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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