Johnson & Johnson Vision Care recalls 1-Day ACUVUE MOIST Daily Wear contact lenses with a partially formed lens that may appear smaller, thicker, and darker blue. Consumers should check lot numbers and contact the company for remedy.
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 the touch and more darkly tinted blue than the normal contact lens.
Johnson & Johnson Vision Care is recalling a specific batch of 1-Day ACUVUE MOIST Daily Wear contact lenses that may have a partially formed lens. This can cause the lens to appear smaller, thicker, and more darkly tinted blue than normal. Using these lenses could lead to discomfort or eye injury.
The recalled lenses may be partially formed, making them appear smaller, thicker, and more darkly tinted blue than normal. This can cause discomfort, eye irritation, or potential injury if the lens does not fit properly.
Contact lens wearers who purchased the recalled 1-Day ACUVUE MOIST Daily Wear lenses with specific lot numbers from the US, Puerto Rico, Canada, Barbados, Korea, or Japan. People with sensitive eyes or those who use contact lenses daily are at higher risk.
Check the lot numbers: Master Lot 516191, 90-Packs with lot numbers 5165915104 (US, PR, Canada, Barbados) or 5165915110 (Japan) or 5165915101 (Korea and Japan). Also look for the Unique Device Identifier (UDI) codes: 733905577215, 733905615078, or 733905888472.
Look for the Master Lot Number 516191 or 90-Pack Lot Numbers listed for your region (US, PR, Canada, Barbados, Korea, or Japan).
Reach out to Johnson & Johnson Vision Care for instructions on returning or replacing the lenses.
The recalled lenses may be partially formed, appearing smaller, thicker, and more darkly tinted blue than normal, which can cause discomfort or eye injury.
Check the lot numbers: Master Lot 516191, 90-Pack Lot Numbers 5165915104 (US, PR, Canada, Barbados), 5165915110 (Japan), or 5165915101 (Korea and Japan), and Unique Device Identifiers 733905577215, 733905615078, or 733905888472.
No, but you should check if you have the recalled lot numbers and contact the manufacturer for instructions.
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-2916-2018 — Johnson & Johnson Vision Care Johnson & Johnson Vision Care Hello, I own a Johnson & Johnson Vision Care that is covered by recall Z-2916-2018 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.
