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Staar Surgical Co. recalls STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses.
Recalled June 22, 2016 · FDA recall Z-1964-2016 · Staar Surgical
Hazard
The STAAR AQ Cartridge-FP may malfunction and may crack during loading or delivery of the IOL (Intraocular Lenses). · FDA Class II
Units
2,612 units
Sold at
US
Description
The STAAR AQ Cartridge-FP may malfunction and may crack during loading or delivery of the IOL (Intraocular Lenses).
Product
STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses.
Manufacturer(s)
Staar Surgical Co.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →