RecallRadar

FDA Drug recall D-0182-2023

Advil Liqui Gels, Solubilized ibuprofen capsules, 200mg, Pain Reliever Fever Reducer (NSAID), 200 liquid filled capsules, Distributed by: P…

On 2023-02-01 the FDA classified a Class I recall of Advil Liqui Gels, Solubilized ibuprofen capsules, 200mg, Pain Reliever Fever Reducer (NSAID), 200 liquid filled capsules, Distributed by: P… by Glaxosmithkline Consumer Healthcare Holdings, citing labeling: Illegible Label; the adhesive migrated onto a portion of the label, causing it to tear when peeled back.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0182-2023
ClassificationClass I
Statusterminated
Initiated2022-12-06
Published2023-02-01
Last updated2026-09-13 11:52 UTC
CompanyGlaxosmithkline Consumer Healthcare Holdings
DistributionUS

Product

Advil Liqui Gels, Solubilized ibuprofen capsules, 200mg, Pain Reliever Fever Reducer (NSAID), 200 liquid filled capsules, Distributed by: Pfizer, Madison, NJ 07940, UPC 3 0573 0169 49 3

Reason

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

Identifiers

upc305730169493
code_infoLot: R94065, Exp 02/29/2024

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0182-2023%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.