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Johnson & Johnson Surgical Vision, Inc. recalls TECNIS Toric II OptiBlue IOL Models ZCW
Recalled January 24, 2024 · FDA recall Z-0735-2024 · Johnson & Johnson Surgical Vision
Hazard
Due to intraocular lens containing an angle out of specification (OOS). The cylinder axis marks do not meet product specifications for the allowable angle between Low Power Meridian (LPM) and toric cylinder axis marks. · FDA Class II
Units
36
Sold at
International distribution to the country of Japan.
Description
Due to intraocular lens containing an angle out of specification (OOS). The cylinder axis marks do not meet product specifications for the allowable angle between Low Power Meridian (LPM) and toric cylinder axis marks.
Product
TECNIS Toric II OptiBlue IOL Models ZCW
Manufacturer(s)
Johnson & Johnson Surgical Vision, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →