A Bunch of Robitussin Cough Syrup Was Just Recalled Due to Microbial Contamination

Health Information Relationships

We’re in the midst of cold and flu season—not to mention a spike in COVID cases—so it’s likely that you’ve recently stocked your medicine cabinet with over-the-counter medicine to help you deal. If your stash includes any Robitussin, you might want to check your bottles: Some kinds of its cough syrups were just recalled following reports of microbial contamination.

On January 24, Haleon—the company that produces Robitussin and other health products, including Sensodyne and Flonase—just recalled eight lots of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult, according to the Food and Drug Administration (FDA). These products are often used to treat common cold and flu symptoms, like coughing, fever, and sore throat.

The following eight lots have been recalled—six are the daytime version, and the remaining two are the nighttime formula. Look for the following lot numbers (which you can find on the bottom right on the back label) on your bottles for Robitussin Honey CF Max Day Adult:

  • T10810
  • T08730
  • T08731
  • T08732
  • T08733
  • T10808

The two recalled lots for Robitussin Honey CF Max Nighttime Adult are T08740 and T08742.

While no cases of adverse effects have been reported, it’s especially important for immunocompromised people to avoid or stop using this product because it could cause them potentially life-threatening infections, including fungemia (fungi or yeast in the blood) or disseminated fungal infection (a term for a group of fungal infections throughout the body), per the FDA. Although severe infections are unlikely in non-immunocompromised people, it’s still a good idea to err on the side of caution and toss these products out, according to the FDA’s announcement.

If you’re experiencing any side effects related to the use of the above products, please contact a doctor or visit your nearest emergency room. You can also report any adverse reactions to the FDA’s MedWatch Adverse Reporting program online here.




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