Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL Recalled by Johnson & Johnson Vision Care, Inc. Due to Due to defects (bubbles/voids) identified during standard finished...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Johnson & Johnson Vision Care, Inc. directly.
Affected Products
ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL
Quantity: 114,165 lenses
Why Was This Recalled?
Due to defects (bubbles/voids) identified during standard finished goods testing
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Johnson & Johnson Vision Care, Inc.
Johnson & Johnson Vision Care, Inc. has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report