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Johnson & Johnson Vision Care, Inc.

Complete recall history across all FDA and CPSC categories — 10 total recalls

Johnson & Johnson Vision Care, Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (10)

FDA medical device enforcement actions by Johnson & Johnson Vision Care, Inc.

Date Product Reason Class
Jun 12, 2025 ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL Due to defects (bubbles/voids) identified during standard finished goods testing Class II
May 6, 2021 ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear. Base... Potential that a limited number of individual contact lens packages have an i... Class II
Mar 11, 2019 ACUVUE OASYS for ASTIGMATISM brand contact lenses, Base Curve 8.6 Refractive ... One lot of ACUVUE OASYS¿ for ASTIGMATISM Brand Contact lenses has the potenti... Class II
Jul 23, 2018 Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve... Johnson and Johnson Vision Care received a number of reports of a partially f... Class II
Dec 18, 2017 ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G. Base Cur... Package integrity failure observed during routine shift package integrity tes... Class II
Oct 19, 2017 1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses Some contact lenses were associated with complaints of a foreign matter caugh... Class II
Oct 19, 2017 ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS Some contact lenses were associated with complaints of a foreign matter caugh... Class II
Oct 19, 2017 ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR Some contact lenses were associated with complaints of a foreign matter caugh... Class II
Dec 21, 2012 1-DAY ACUVUE MOIST Brand Contact Lenses, soft disposable contact lenses. T... Limited number of individual contact lens packages may not have been complete... Class II
Dec 21, 2012 ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR, Soft, disposable contact... Limited number of individual contact lens packages may not have been complete... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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