PlainRecalls
FDA Drug Critical Class I Ongoing

Robitussin Honey CF Max Non-Drowsy Adult (Acetaminophen 650mg, Dextromethorphan HBr 20 mg), a) 4 FL OZ (118mL) and b) 8 FL OZ (237 mL) bottles, Distributed by: GSK Consumer Healthcare, Warren, NJ 07059

Reported: January 31, 2024 Initiated: December 26, 2023 #D-0316-2024

Product Description

Robitussin Honey CF Max Non-Drowsy Adult (Acetaminophen 650mg, Dextromethorphan HBr 20 mg), a) 4 FL OZ (118mL) and b) 8 FL OZ (237 mL) bottles, Distributed by: GSK Consumer Healthcare, Warren, NJ 07059

Reason for Recall

Microbial Contamination of Non-Sterile Products

Details

Recalling Firm
Haleon US Holdings LLC
Units Affected
a) 31,632 bottles; b) 336,528 bottles
Distribution
USA nationwide
Location
Warren, NJ

Frequently Asked Questions

What product was recalled?
Robitussin Honey CF Max Non-Drowsy Adult (Acetaminophen 650mg, Dextromethorphan HBr 20 mg), a) 4 FL OZ (118mL) and b) 8 FL OZ (237 mL) bottles, Distributed by: GSK Consumer Healthcare, Warren, NJ 07059. Recalled by Haleon US Holdings LLC. Units affected: a) 31,632 bottles; b) 336,528 bottles.
Why was this product recalled?
Microbial Contamination of Non-Sterile Products
Which agency issued this recall?
This recall was issued by the FDA Drug on January 31, 2024. Severity: Critical. Recall number: D-0316-2024.