Johnson & Johnson Vision Care recalls ACUVUE VITA daily contact lenses with Base Curve 8.8 and Refractive Power -1.50 due to potential incomplete packaging seals. Consumers should check UPC 733905989612 and lot number BOOWWWL.
Potential that a limited number of individual contact lens packages have an incomplete packaging seal.
Johnson & Johnson Vision Care is recalling ACUVUE VITA soft contact lenses for daily wear with specific measurements. The recall is due to a potential incomplete packaging seal, which could lead to contamination or improper storage.
An incomplete packaging seal could allow contaminants to enter the lens package, increasing the risk of eye infections or improper lens storage. This is a potential contamination hazard rather than an immediate safety risk.
Contact lens wearers who purchased ACUVUE VITA soft lenses with Base Curve 8.8 and Refractive Power -1.50. Those who use the lenses daily are most at risk if the packaging seal is incomplete.
Check for the UPC 733905989612 and lot number BOOWWWL on the packaging. The lenses are for daily wear with Base Curve 8.8 and Refractive Power -1.50.
Inspect the packaging seal for completeness; if it appears damaged or missing, do not use the lenses.
The recall is due to a potential incomplete packaging seal in a limited number of ACUVUE VITA contact lens packages, which could lead to contamination.
Look for the UPC 733905989612 and lot number BOOWWWL on the packaging. The lenses have Base Curve 8.8 and Refractive Power -1.50 for daily wear.
Inspect the packaging seal; if it appears damaged or missing, do not use the lenses. The remedy does not specify a return or disposal process.
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-1865-2021 — Johnson & Johnson Vision Care Johnson & Johnson Vision Care Hello, I own a Johnson & Johnson Vision Care that is covered by recall Z-1865-2021 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.
