New major recall of the Robutin cough syrup for "contamination", warns the FDA
Eight lots were fired after finding that the drug could put people at risk of infections.
As a child, you may have dreaded by taking Robutinssin, who did not necessarily have the most attractive taste. Even so, we cannot deny its effectiveness when processing a cough, and it is always something that most of us keep around the house during Cold and flu season . But while Robitinssin remains one of the most reliable names in over -the -counter medicines, you will return to the bottle you have in your pharmacy cabinet, thanks to a new reminder.
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In a January 24 alert From the US Food and Drug Administration (FDA), the consumer health company Haleon has announced that eight lots of Robutin Honey Cf Max Day Adult and Robitin Honey CF Max Nighttime Adult has been recalled. Both are used to treat symptoms related to colds or flu, hay fever and other respiratory allergies, according to the FDA. On the packaging of drugs, he specifically notes the control of cough and the relief of a flowing nose, sneezing, fever and body pain.
According to the FDA alert, Robutassin products have been recalled due to "microbial contamination". For those who are immunocompromised, the use of these Robitinin products "could potentially cause severe or potentially fatal undesirable events such as fungal or a disseminated fungal infection," said the agency.
According to the National Library of Medicine, fungal is the presence of mushroom . The most common type is candidemic , which can lead to "long stays in the hospital and death", according to the Centers for Disease Control and Prevention (CDC).
For those who are not immunocompromised, which the agency quotes as "the population most likely to use the product", the recalled Robutussin is likely to cause a potentially fatal infection. However, these people could still develop an infection that requires medical intervention.
Robitinin Honey Cf Max Day Liquids was sold in bottles of four ounces and eight ounces, with exposure dates between May 31, 2025 and September 30, 2025. The night version was sold in bottles of eight ounces, which have an expiration date of June 30, 2026. A complete list of specific lots and expiration dates is included in the FDA alert. On the Robitin Bottles, the Lot code and the expiration date are printed on the rear label, in the lower right corner.
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If you have recalled Robitinin products at home, the FDA asks you to "stop consumption immediately" and contact your health care provider if you encounter medication problems. Haleon had not received any report of adverse events linked to the product on January 24.
The company directly informs distributors and recall customers and includes instructions to return the affected products, indicates the opinion of the FDA. Consumers can also call the Haleon customer relations team at 1-800-245-1040, Monday to Friday between 8 a.m. and 6 p.m. Eastern (and) hour, or email [Protected by e-mail] With direct questions.
In addition, the FDA is asking you to report quality problems or unwanted events to its MEDWatch adverse event reports. You can do it by fill out an online form , or by ordinary mail or fax. Download the form Online or call 1-800-332-1088 to request a report form.
