FDA-Device2025-07-30Class II
ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL
Johnson & Johnson Vision Care, Inc.
Hazard
Due to defects (bubbles/voids) identified during standard finished goods testing
Sold states
Worldwide - U.S. Nationwide distribution including in the states of AL, AZ, CA, CO, DE, FL, GA, HI, IA, IL, IN, KN, KS, KY, LA, MA, MD, MI, MO, NC, NJ, NV, NY, OH, PA, SC TN, TX, UT, VA, WA, WI, and WY. The countries of Belgium, Bermuda, Canada, Switzerland, Denmark, Germany, Spain, France, United Kingdom, Italy, Netherlands, Poland, Sweden, Singapore, and South Korea.
Affected count
114,165 lenses
Manufactured in
7500 Centurion Pkwy, N/A, Jacksonville, FL, United States
Products
ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2163-2025Don't want to check this manually?
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