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DOH Issues Voluntary Recall for Certain Robitussin Honey Cough Syrup Products

The Hawai‘i State Department of Health (DOH) Food and Drug Branch is alerting residents to a voluntary recall by Haleon, manufacturer of Robitussin cough syrups. Specifically, eight lots of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult cough syrup products are being recalled due to microbial contamination.
Immunocompromised individuals who use the affected product could potentially develop severe or life-threatening adverse effects, such as fungemia or disseminated fungal infection. Life-threatening infections are not likely to occur with non-immunocompromised individuals, however, the occurrence of an infection may necessitate medical intervention.
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using the product. To date, there have been no reports of adverse events attributed to the recalled products.
The DOH Food and Drug Branch is advising customers to check the Lot Number and Expiration Date to determine if they possess the recalled product. At that time they should stop consumption and safely dispose of the product or return it to place of purchase for a refund.
For more information, contact Haleon Customer Relations at 1-800-245-1040 (3:00 a.m. to 1:00 p.m. HST, Monday through Friday) or via email at mystory.us@haleon.com.
Product descriptions and relevant information are listed below:

Product  Lot Number  Exp. Date 
ROBITUSSIN HONEY CF MAX DAY ADULT 4oz T10810 31OCT2025
ROBITUSSIN HONEY CF MAX DAY ADULT 8oz T08730 31MAY2025
T08731 31MAY2025
T08732 31MAY2025
T08733 31MAY2025
T10808 30SEP2025
ROBITUSSIN HONEY CF MAX NT ADULT 8oz T08740 30JUN2026
T08742 30JUN2026

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