Johnson & Johnson Vision Care ACUVUE OASYS MAX 1-Day MULTIFOCAL recall — FDA Z-2163-2025
Due to defects (bubbles/voids) identified during standard finished goods testing
Overview of recall records associated with Johnson & Johnson Vision Care, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 4.
Due to defects (bubbles/voids) identified during standard finished goods testing
Potential that a limited number of individual contact lens packages have an incomplete packaging seal.
One lot of ACUVUE OASYS for ASTIGMATISM Brand Contact lenses has the potential for a limited number of individual contact lens packages to have an incomplete packaging seal.
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…
This page summarizes recall records in which the official source identifies Johnson & Johnson Vision Care, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.