PlainRecalls
FDA Drug Critical Class I Ongoing

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

Reported: January 31, 2024 Initiated: December 26, 2023 #D-0317-2024

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

Details

Recalling Firm
Haleon US Holdings LLC
Units Affected
21,900 bottles
Distribution
USA nationwide
Location
Warren, NJ

Frequently Asked Questions

What product was recalled?
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. Recalled by Haleon US Holdings LLC. Units affected: 21,900 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-0317-2024.