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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Johnson & Johnson Vision Care, Inc.: Some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil.

Agency Publication Date: March 27, 2018
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Affected Products

Product: ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS

Lot L002NCS exp. 05/2020 base Curve 8.8 Refractive Power -4.00D and Lot L002QH9 exp. 08/2020 Base Curve 8.8 Refractive Power -4.50D Manufactured at J&J Vision Care Ireland

Lot Numbers:
L002NCS
L002QH9
Product: ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR

Lot B00DHLP Exp. 08/2018 Base Curve 8.7, Refractive Power -10.00D - Manufactured in J&J Vision Care Inc. Jacksonville, FL Lot L002FNL Exp. 07/2020 Base Curve 8.7 Refractive Power -4.75D Manufactured in J&J Vision Care Ireland Lot L002V94 Exp. 01/2022 Base Curve 8.7 Refractive Power -5.00D

Lot Numbers:
B00DHLP
L002FNL
L002V94
Product: 1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses

Lot B00LF41 Exp. 04/2021 Base Curve 8.5 Refractive Power -7.50D -1.25/180 Manufactured at J&J Vision Care Inc. Jacksonville, FL

Lot Numbers:
B00LF41

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 79152
Status: Resolved
Manufacturer: Johnson & Johnson Vision Care, Inc.
Manufactured In: United States
Units Affected: 3 products (125,763; 165,750; 56,070)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.