top of page

Recall: Robitussin Honey CF Max Day Adult AND Honey CF Max Nighttime Cough Syrup: Microbial Contamination

Updated: Jan 29

1/24/24 Haleon is voluntarily recalling eight lots of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult cough syrup due to microbial contamination.


In immunocompromised individuals, the use of the affected product could potentially result in severe or life-threatening adverse events such as fungemia or disseminated fungal infection. In non-immunocompromised consumers, the population most likely to use the product, life-threatening infections are not likely to occur. However, the occurrence of an infection that may necessitate medical intervention cannot be completely ruled out.

To date, Haleon has not received any reports of adverse events related to this recall.


Robitussin Honey CF Max Day and Nighttime are cough syrups indicated for the temporary relief of symptoms occurring with cold or flu, hay fever, or other respiratory allergies. This recall covers only the following lots:

Product

Lot Number

Expiry Date

ROBITUSSIN HONEY CF MAX


DAY ADULT 4OZ

T10810

31OCT2025

ROBITUSSIN HONEY CF MAX


DAY ADULT 8OZ

T08730


T08731


T08732


T08733


T10808

31MAY2025


31MAY2025


31MAY2025


31MAY2025


30SEP2025

ROBITUSSIN HONEY CF MAX


NT ADULT 8OZ

T08740 T08742

30JUN2026


30JUN2026

Haleon is notifying its distributors and customers directly and has provided them with instructions for the return of all recalled products.


ACTION

Consumers that have purchased the product listed should stop consumption immediately.


CONTACT

Please call our Consumer Relations team at +1-800-245-1040 (Monday through Friday 8 AM to 6 PM Eastern Time) or reach out via email to mystory.us@haleon.com.


Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.


Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.


bottle showing lot nuber
Robitussin bottle

11 views

Comments


bottom of page