Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear Recalled by Johnson & Johnson Vision Care, Inc. Due to Johnson and Johnson Vision Care received a number...
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
Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve, -3.25 Power. Master Lot, containing 12 split lots, repackaged in 30 and 90-packs . Intended for daily disposable wear for the optical correction of refractive ametropia (myopia and hyperopia) in phakic or aphakic persons with non-diseased eyes who may have 1.00D or less of astigmatism.
Quantity: 195,660 Total; 89,640 US & Puerto Rico, 106,020 OUS
Why Was This Recalled?
Johnson and Johnson Vision Care received a number of reports of a partially formed contact lens, which appears to the customer or consumer as visibly smaller in diameter, thicker/stiffer to the touch and more darkly tinted blue than the normal contact lens.
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