Robitussin Recall Due To Microbial Contamination

The maker of Robitussin, Haleon, announced the recall of eight lots of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult due to microbial contamination.

Haleon says that the use of the affected product could potentially result in severe or life-threatening adverse events such as fungemia or disseminated fungal infection to immune-compromised consumers. 

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 Recall 2024

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:

The recall specifically applies to the following lots of Robitussin Honey CF Max Day and Nighttime cough syrups:

ROBITUSSIN HONEY CF MAX DAY ADULT 4OZ: Lot Number T10810, Expiry Date 31OCT2025

ROBITUSSIN HONEY CF MAX DAY ADULT 8OZ: Lot Numbers T08730, T08731, T08732, T08733, T10808, Expiry Date 31MAY2025 and 30SEP2025

ROBITUSSIN HONEY CF MAX NIGHTTIME ADULT 8OZ: Lot Numbers T08740, T08742, Expiry Date 30JUN2026

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

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

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