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Advil Liqui Gels (minis), Solubilized ibuprofen capsules, 200mg, Pain Reliever Fever Reducer (NSA...

FDA Recall #D-0183-2023 — Class I — December 6, 2022

Recall #D-0183-2023 Date: December 6, 2022 Classification: Class I Status: Terminated

Product Description

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

Reason for Recall

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

Recalling Firm

Glaxosmithkline Consumer Healthcare Holdings DBA Haleon — Warren, NJ

Classification

Class I — Reasonable probability of serious adverse health consequences or death.

Product Type

Drugs

Product Quantity

209,292 capsules

Distribution

Nationwide in the USA.

Code Information

Lot: R93517, R94072, R94073, Exp 02/29/2024; T00655, Exp 03/31/2025

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.

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