Robitussin Honey CF Max Nighttime Adult (Acetaminophen 650 mg, Diphenhydramine HCl 25mg), 8 FL OZ...

FDA Recall #D-0317-2024 — Class I — December 26, 2023

Recall #D-0317-2024 Date: December 26, 2023 Classification: Class I Status: Ongoing

Product Description

Robitussin Honey CF Max Nighttime Adult (Acetaminophen 650 mg, Diphenhydramine HCl 25mg), 8 FL OZ (237 mL) bottle, Distributed by: GSK Consumer Healthcare, Warren, NJ 07059

Reason for Recall

Microbial Contamination of Non-Sterile Products

Recalling Firm

Haleon US Holdings LLC — Warren, NJ

Classification

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

Product Type

Drugs

Product Quantity

21,900 bottles

Distribution

USA nationwide

Code Information

Lot#: T08740, T08742, Exp 06/30/2026

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated