HEALTH
Why the FDA is recalling Robitussin cough syrup: is it harmful to health?
Eight lots of Robitussin cough syrup are being recalled due to contamination though no deaths have been reported.
Health company Haleon is recalling eight lots of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult after concerns were flagged by the FDA.
Robitussin is a brand of over-the-counter cough and cold medications produced by Pfizer Consumer Healthcare. The active ingredient in many Robitussin products is dextromethorphan, which helps relieve coughing.
These are the affected medications:
| Product | Lot Number | Expiry Date |
|---|---|---|
| ROBITUSSIN HONEY CF MAXDAY ADULT 4OZ | T10810 | Oct. 31, 2025 |
| ROBITUSSIN HONEY CF MAXDAY ADULT 8OZ | T08730 T08731 T08732 T08733 T10808 |
May 31, 2025 May 31, 2025 May 31, 2025 May 31, 2025 Sept. 30, 2025 |
| ROBITUSSIN HONEY CF MAXNT ADULT 8OZ | T08740 T08742 |
June 30, 2026 June 30, 2026 |
Why is it being recalled?
The FDA reported that the products are bring recalled because of microbial contamination. At this stage there are no reports of illness related to the products.
If problems are suffered then the FDA advises to contact them at www.fda.gov/medwatch/report.htm or call at 1-800-332-1088.