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Class I · Most seriousRecall completed

Advil Liqui Gels (minis)

A reasonable chance it could cause serious harm or death.

Does this affect you?
Check your lot numberLot: R93517, R94072, R94073, Exp 02/29/2024; T00655, Exp 03/31/2025
Where it was soldNationwide in the USA.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Labeling: Illegible Label; the adhesive migrated onto a portion of the label, causing it to tear when peeled back

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Distributed by / forGlaxosmithkline Consumer Healthcare Holdings DBA Haleon
Show the full FDA record
Full product labelAdvil Liqui Gels (minis), Solubilized ibuprofen capsules, 200mg, Pain Reliever Fever Reducer (NSAID), 200 liquid filled capsules, Pfizer, Madison, NJ 07940, UPC 3 0573 1769 13 5
Recalling firmGlaxosmithkline Consumer Healthcare Holdings DBA Haleon
DistributionNationwide in the USA.
Quantity209,292 capsules
Recall initiated2022-12-06
Report date2023-02-01
Recall completed2024-02-26
Recall numberD-0183-2023
ClassificationClass I
FDA statusTerminated
Origin on fileWarren NJ United States

Related

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Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.