← FDA ENFORCEMENT
D-0317-2024Class I

Haleon US Holdings LLC

Recalling firm
Haleon US Holdings LLC
Product type
Drug
Status
Ongoing
Report date
2024-01-31
Distribution
USA nationwide
Firm state
NJ
Product quantity
21,900 bottles
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

Microbial Contamination of Non-Sterile Products

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

Code / lot info

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

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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.