FDAJune 12, 2025device

ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL

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

The hazard

Due to defects (bubbles/voids) identified during standard finished goods testing

What to do

FDA enforcement status: Ongoing

Brands named

johnson johnson vision carejohnsonjohnson johnson

UPCs

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Recall history

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

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