FDADecember 12, 2023device

TECNIS Toric II OptiBlue IOL Models ZCW

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

johnson johnson surgical visionjohnsonjohnson johnson

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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