Haleon recalls Advil Liqui Gels minis due to labels becoming illegible after adhesive migration. Consumers should check product labels and contact Haleon for details.
Labeling: Illegible Label; the adhesive migrated onto a portion of the label, causing it to tear when peeled back
Haleon is recalling Advil Liqui Gels minis because the labels become illegible when the adhesive migrates and tears. This could make it hard to identify the product correctly, but it doesn't pose a safety risk.
The adhesive on the label migrates and causes the label to tear when peeled back. This makes the label illegible, which could lead to confusion about the product's contents or expiration date.
Owners of Advil Liqui Gels minis with specific lot numbers and expiration dates are affected. People who rely on these products for pain relief may need to check their labels.
Check for lot numbers R93517, R94072, R94073 with expiration dates of 02/29/2024 or 03/31/2025. The product is a 200mg liquid-filled capsule labeled as Advil Liqui Gels minis.
Inspect the label for tearing or illegible text caused by adhesive migration.
The label becomes illegible due to adhesive migration and tearing when peeled back, which could cause confusion about the product's contents.
Look for lot numbers R93517, R94072, R94073 with expiration dates of 02/29/2024 or 03/31/2025.
The recall does not require stopping use; check the label condition and contact Haleon for further details.
We’ve drafted a message you can send Haleon to request your refund or repair — edit it as you like.
Subject: Recall D-0183-2023 — Haleon Haleon Hello, I own a Haleon that is covered by recall D-0183-2023 from Haleon. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
