Alcon Research, Ltd.: Medical Device Recall in 2017 - (Recall #: Z-0978-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Alcon Monarch III (1) "C" Cartridge The device is used for implanting AcrySof intraocular lenses in the eye following cataract removal

Product Classification:

Class II

Date Initiated: September 5, 2016

Date Posted: January 18, 2017

Recall Number: Z-0978-2017

Event ID: 75049

Reason for Recall:

The intraocular lens could become lodged within the cartridge

Status: Terminated

Product Quantity: 1,130 units

Code Information:

Alcon Monarch II C Cartridge Model 8065977762, Lot Number 32395407, Manufacture Date 8/13/2015

Distribution Pattern:

Distributed to Mexico only

Voluntary or Mandated:

Voluntary: Firm initiated