Johnson & Johnson Vision Care recalls ACUVUE OASYS MAX 1-Day Multifocal contact lenses with bubbles/voids found during testing. Consumers should check product details to determine if affected.
Due to defects (bubbles/voids) identified during standard finished goods testing
Johnson & Johnson Vision Care is recalling ACUVUE OASYS MAX 1-Day Multifocal contact lenses due to defects (bubbles or voids) identified during standard testing. These defects could potentially cause lens failure or discomfort during use.
The lenses have bubbles or voids in the material that were detected during standard finished goods testing. These defects could lead to lens failure or discomfort during wear, but they do not pose a risk of injury or damage to the eye.
Contact lens wearers who purchased ACUVUE OASYS MAX 1-Day Multifocal lenses with the specific lot numbers listed in the recall notice. People with high prescription needs or sensitive eyes may be at slightly higher risk.
Check the product label for the specific lot numbers listed in the recall notice: J003QC7, J003QC8, J003QC9, J003QCB, J003QCC, J003QCD, J003QCG, J003QCH, J003QCJ, J003QHP, J003QCK, J003Q71, J003Q72, J003Q73, J003Q74, J003QHT, J003Q75, J003QCL, J003QCM, J003Q76, J003QCQ, J003QD0, J003QM9, J003QD3, J003QD4, J003QD5, J003QD9, J003QDG, J003QDH, J003QDK, J003QHW, J003QBT, J003QCV, J003QQH, J003QBX, and V00D228 (J003QHT).
Look for the specific lot numbers listed in the recall notice to determine if your lenses are affected.
The recall is due to defects (bubbles or voids) found during standard testing, but the lenses are generally safe for use. Consumers should check the product label for specific lot numbers to determine if affected.
Check the product label for the specific lot numbers listed in the recall notice. If affected, contact Johnson & Johnson Vision Care for further instructions.
Look for the specific lot numbers listed in the recall notice: J003QC7, J003QC8, J003QC9, J003QCB, J003QCC, J003QCD, J003QCG, J003QCH, J003QCJ, J003QHP, J003QCK, J003Q71, J003Q72, J003Q73, J003Q74, J003QHT, J003Q75, J003QCL, J003QCM, J003Q76, J003QCQ, J003QD0, J003QM9, J003QD3, J003QD4, J003QD5, J003QD9, J003QDG, J003QDH, J003QDK, J003QHW, J003QBT, J003QCV, J003QQH, J003QBX, and V00D228 (J003QHT).
We’ve drafted a message you can send Johnson & Johnson Vision Care to request your refund or repair — edit it as you like.
Subject: Recall Z-2163-2025 — Johnson & Johnson Vision Care Johnson & Johnson Vision Care Hello, I own a Johnson & Johnson Vision Care that is covered by recall Z-2163-2025 from Johnson & Johnson Vision Care. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
