Johnson & Johnson Vision Care recalls 1-Day ACUVUE Moist contact lenses with foreign matter complaints between blister and foil. Affected lot B00LF41 expiring 04/2:2021. No remedy specified in recall notice.
Some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil.
Johnson & Johnson Vision Care is recalling 1-Day ACUVUE Moist contact lenses that may have foreign matter caught between the blister package and foil. This could cause discomfort or eye irritation if the lenses are used.
Foreign matter can get stuck between the blister package and foil, potentially causing discomfort or irritation when the lenses are used. This is not a serious injury risk but may lead to eye irritation.
Contact lens wearers who purchased the affected lot B00LF41 (expiring 04/2021) are likely affected. People with astigmatism using these specific lenses are at higher risk due to the product's design.
Check for the lot number B00LF41 on the packaging. The lenses expire April 2021 and have a base curve of 8.5 with refractive power -7.50D -1.25/180.
Look for the lot number B00LF41 on the packaging to identify affected lenses.
The recall is due to potential foreign matter between the blister and foil, which may cause discomfort but is not a serious injury risk.
Check the packaging for lot number B00LF41; if you have it, contact Johnson & Johnson Vision Care for guidance.
The recall notice does not specify a remedy, so no action is required beyond checking the packaging.
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-1211-2018 — Johnson & Johnson Vision Care Johnson & Johnson Vision Care Hello, I own a Johnson & Johnson Vision Care that is covered by recall Z-1211-2018 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.
