Staar Surgical Co.: Medical Device Recall in 2016 - (Recall #: Z-1964-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses.

Product Classification:

Class II

Date Initiated: May 2, 2016

Date Posted: June 22, 2016

Recall Number: Z-1964-2016

Event ID: 74067

Reason for Recall:

The STAAR AQ Cartridge-FP may malfunction and may crack during loading or delivery of the IOL (Intraocular Lenses).

Status: Terminated

Product Quantity: 2,612 units

Code Information:

1281706, 1282812

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated