Bausch & Lomb Surgical, Inc.: Medical Device Recall in 2014 - (Recall #: Z-1062-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos IOL intended for primary implantation in the capsular bag of the eye for the visual correction of aphakia secondary to the removal of a cataractous lens in adult patients.

Product Classification:

Class II

Date Initiated: October 16, 2013

Date Posted: February 26, 2014

Recall Number: Z-1062-2014

Event ID: 67283

Reason for Recall:

Lens was manufactured with incorrect raw material.

Status: Terminated

Product Quantity: 336 IOLs (283 IOLs in the US, 53 IOLs outside the US)

Code Information:

Model Numbers(s): AO60 and MI60L

Distribution Pattern:

Worldwide Distribution: US (nationwide) and Internationally to: Great Britain, France, Spain, Portugal, Sweden, Russia and Guadeloupe.

Voluntary or Mandated:

Voluntary: Firm initiated