Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear. Recalled by Johnson & Johnson Vision Care, Inc. Due to Potential that a limited number of individual contact...
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 VITA soft (hydrophilic) contact lens (spherical) for daily wear. Base Curve 8.8, Refractive Power -1.50
Quantity: 6,780 lenses
Why Was This Recalled?
Potential that a limited number of individual contact lens packages have an incomplete packaging seal.
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