(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.