Reported Aug 29, 2018 · Terminated

Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve, -3.25 Power. Master Lot, containing 12…

Johnson & Johnson Vision Care, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Johnson & Johnson Vision Care, Inc. · 7500 Centurion Pkwy · Jacksonville, FL · 32256-0517

Is this the product you have?

  • 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.
Lot codes and dates

4 of 4 products

Products covered by this recall
#BarcodesProduct as published
1Lot Number (Japan) 5165915110 which contains 30 pack
2lot numbers: 5165910110, 5165910111, 5165910112. 90 Pack
3Lot Number (Korea and Japan) 5165915101 which contains 30 pack
4733905577215733905615078733905888472lot numbers: 5165910101, 5165910102, 5165910103. Unique Device Identifier (UDI): 733905577215, 733905615078, and 733905888472.
Amount recalled
195,660 Total; 89,640 US & Puerto Rico, 106,020 OUS

Where it was sold

Why it was 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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Dec 6, 2021 · Data as of Sep 19, 5:25 PM UTC

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