Hareon is Reminds me of 8 lots of Robitussin cough syrup According to a notice posted by , it was sold nationwide due to microbial contamination. US Food and Drug Administration Wednesday.
According to Haleon, Robitusin Honey CF Max Daytime and Nighttime is a cough syrup charged with the purpose of temporarily relieving symptoms caused by colds and flu, hay fever and other respiratory allergies.
According to Haleon, use of the affected products may result in serious or life-threatening adverse events such as fungemia and disseminated fungal infections in immunocompromised people.
The notice states that although life-threatening infections are unlikely to occur in people who are not immunocompromised, the occurrence of infections that may require medical intervention “cannot be completely ruled out.”
To date, Haleon has not received any reports of adverse events related to this call, according to the FDA notice.
USA TODAY Recall Database:Get the latest product recall information in our database
Which Robitusin products are subject to recall?
Only the following lots are subject to the recall:
| product | Reference number | date of expiry |
| Robitussin Honey CF Maxday Adult 4oz | T10810 | October 31, 2025 |
| Robitussin Honey CF Maxday Adult 8oz | T08730T08731T08732T08733T10808 | May 31, 2025 May 31, 2025 May 31, 2025 September 2025 30, 2025 |
| Robitussin Honey CF MAXNT Adult 8oz | T08740 T08742 | June 30, 2026June 30, 2026 |
Consumers who have purchased the affected product should immediately discontinue use and contact their health care provider if they experience any problems that may be related to ingestion or use of this product.
Consumers with questions can contact Haleon by phone at 1-800-245-1040 or email at [email protected].
