Haleon Issues Voluntary Nationwide Recall Due to Microbial Contamination

In Warren, NJ, Haleon is recalling eight lots of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult due to microbial contamination.

Consumers who have purchased the products listed should cease consumption immediately. Haleon has notified its distributors and customers directly and instructed them to return the recalled products.

A severe or life-threatening adverse event such as fungemia or disseminated fungal infection may result from the use of the affected product in immunocompromised individuals. The population most likely to use the product is non-immunocompromised, so there is a lower risk of life-threatening infections. However, an infection that requires medical intervention cannot be completely excluded.

Haleon has not received any reports of adverse events associated with this recall.

Cold and flu symptoms, hay fever, and other respiratory allergies may be temporarily relieved with Robitussin Honey CF Max Day and Nighttime cough syrups.

If consumers have experienced any problems after taking or using this product, they should contact their physician or healthcare provider immediately.

The FDA's MedWatch Adverse Event Reporting program allows users to report adverse reactions or quality problems experienced with this product online, by mail, or by fax.

Complete and submit the report
Online: www.fda.gov/medwatch/report.htm
Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form

Recall Product Info