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Robitussin cough syrups recalled due to contamination

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(WHTM) — Two types of Robitussin cough syrups sold nationwide are being voluntarily recalled due to microbial contamination, the U.S. Food and Drug Administration announced Wednesday.

Haleon, which manufactures the medication, is recalling eight lots of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult.

According to the company, immunocompromised individuals who use the affected products “could potentially result in severe or life-threatening adverse events such as fungemia or disseminated fungal infection.”

Those who are not immunocompromised are not likely to experience infections, and no illnesses have been reported to date.

The following lots are impacted by this recall:

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

Those who have an affected product should stop using them and call 1-800-245-1040 or email mystory.us@haleon.com.

If you have experienced any problems using these products, you’re asked to contact your doctor.

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