FDA Class II Recall: ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL by Johnson & Johnson Vision Care, Inc.

Key facts

What consumers should do

Facilities, clinicians, and consumers holding an affected unit or lot of ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL should stop using it for the purpose described in the recall notice and hold remaining stock pending instructions from Johnson & Johnson Vision Care, Inc.. FDA recall records typically direct the recalling firm to notify known accounts directly with a recall letter describing the specific corrective action -- replacement, field correction, refund, or return. Anyone who received the product through a distributor rather than directly from Johnson & Johnson Vision Care, Inc. should confirm with their supplier whether their specific lot or unit is on the affected list, since recall notices are lot- or unit-specific and not every unit of a product line is necessarily included. Questions about a specific unit's status should go to Johnson & Johnson Vision Care, Inc. directly or to the distributor that supplied it; Argus HQ is a public-record aggregator, not the recalling firm, and cannot confirm individual unit status.

What this classification means

A Class II recall is FDA’s middle classification. FDA assigns Class II when use of, or exposure to, the recalled product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote. FDA still requires the recalling firm to notify affected accounts and submit status reports on the correction, though the monitoring intensity is lower than for a Class I recall. FDA's Center for Devices and Radiological Health (for devices) or Center for Drug Evaluation and Research (for drugs) reviews the classification and can require additional corrective action if the initial response is judged insufficient. Because this record is filed as Class II, professionals and consumers handling an affected lot should treat FDA's own classification -- not this page's summary of it -- as the authoritative risk signal. A Class I recall is FDA’s most serious classification. FDA assigns Class I when there is a reasonable probability that use of, or exposure to, the recalled product will cause serious adverse health consequences or death. This classification does not mean harm has already occurred in every case -- it reflects FDA’s assessment of the realistic worst-case risk profile of the defect described in the recall, based on the reason for recall reported by the firm. Class I recalls receive the closest FDA monitoring of the three classes: the recalling firm typically must submit a recall strategy, periodic status reports, and effectiveness checks confirming that the affected lots have actually been removed from distribution or corrected in the field.

Johnson & Johnson Vision Care, Inc.’s FDA history

Argus HQ has recorded 1 total FDA action tied to Johnson & Johnson Vision Care, Inc.: 0 warning letters, 1 recall, 0 approval records, and 0 Form 483 inspection citations.

Frequently asked questions

Where can I verify this recall directly with FDA?

The verbatim FDA record is the source of truth for every recall Argus HQ tracks — always confirm against fda.gov before acting.

Is ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL recalled?

Yes. FDA lists a Class II recall by Johnson & Johnson Vision Care, Inc. for ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL, reported 20250730, with status "Ongoing." FDA recall number: Z-2163-2025.

What is the recall class for Johnson & Johnson Vision Care, Inc.'s recall?

FDA classified this recall as Class II. A Class II recall is FDA’s middle classification. FDA assigns Class II when use of, or exposure to, the recalled product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

Why was ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL recalled?

FDA's recall record states the reason as: Due to defects (bubbles/voids) identified during standard finished goods testing

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