Glaxosmithkline Consumer Healthcare Holdings DBA Haleon recalls Advil Liqui Gels (minis), Solubilized ibuprofen capsules, 200mg, Pain Reliever Fever Reducer (NSAID), 200 liquid filled…

Recall date

December 6, 2022

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0183-2023

FDA classification

Class I

Brand / firm

Glaxosmithkline Consumer Healthcare Holdings DBA Haleon

Sold / distributed

Nationwide in the USA.

Why it was recalled

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

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

Advil 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