Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Akreos Recalled by Bausch & Lomb Surgical, Inc. Due to An off-power error was identified, which resulted in...

Date: June 6, 2025
Company: Bausch & Lomb Surgical, Inc.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Bausch & Lomb Surgical, Inc. directly.

Affected Products

Akreos, SKU: AO60P0300. Akreos intraocular lenses

Quantity: 2

Why Was This 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.

Where Was This Sold?

This product was distributed to 2 states: AZ, CA

Affected (2 states)Not affected

About Bausch & Lomb Surgical, Inc.

Bausch & Lomb Surgical, Inc. has 10 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report