Home / Recalls / Medical Devices
Johnson & Johnson Vision Care, Inc. recalls ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL
Recalled July 30, 2025 · FDA recall Z-2163-2025 · Johnson & Johnson Vision Care
Hazard
Due to defects (bubbles/voids) identified during standard finished goods testing · FDA Class II
Units
114,165 lenses
Sold at
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.
Description
Due to defects (bubbles/voids) identified during standard finished goods testing
Product
ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL
Manufacturer(s)
Johnson & Johnson Vision Care, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →