Robitussin Cold And Flu Cough Syrups Recalled Due to Contamination
OAN’s Brooke Mallory
4:53 PM – Thursday, January 25, 2024
The consumer health company Haleon has issued a nationwide recall of certain Robitussin products, which are commonly used to treat cough, flu, and sore throat symptoms. This recall is due to a microbiological contamination that poses a potential risk to consumers.
With the cold and flu season approaching, this recall couldn’t have come at a worse time.
The recall affects eight lots of Robitussin Honey CF Max Day and Max Night cough syrup, available in four- and eight-ounce bottles. The affected products have expiration dates set for May 2025 or June 2026.
According to the FDA press release, individuals with weakened immune systems may be particularly vulnerable to the contamination, which could lead to serious and potentially fatal conditions such as blood fungal infections.
However, the FDA states that individuals without compromised immune systems are unlikely to be at risk of developing these life-threatening conditions. Nevertheless, there is still a possibility of infection that may require medical intervention.
The recall specifically includes the following lots:
“Consumer safety and product quality are our utmost priorities at Haleon,” the company said in a statement to ABC News on Thursday. “After a thorough investigation, a root cause has been identified, and we are implementing corrective and preventative actions to ensure that this does not recur.”
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What steps has the company taken to address the contamination issue and ensure consumer safety?
Entified, and we are taking swift action to address the issue and ensure the safety of our consumers.”
Haleon has advised consumers who have purchased the affected products to stop using them immediately and return them to the place of purchase for a full refund. Additionally, healthcare professionals and institutions have been urged to quarantine and discontinue the use of any remaining inventory of the recalled Robitussin cough syrups.
The contamination was discovered during routine testing by Haleon, and no adverse events related to the recalled products have been reported so far. The company is working closely with the FDA to resolve the issue and prevent any further incidents.
Consumers are advised to check the lot numbers of any Robitussin Honey CF Max Day and Max Night cough syrups they have purchased and compare them to the list provided in the FDA press release. Lot numbers can typically be found on the label of the product.
For those who have purchased the affected products, it is important to consult with a healthcare professional if they experience any symptoms such as fever, chills, skin rashes, cough, or difficulty breathing.
Although the recall is concerning, it is crucial for consumers to remain vigilant and informed about product recalls. Regularly checking the FDA website or other reliable sources for updates on recalls and taking appropriate actions can help ensure the safety and wellbeing of individuals and their families.
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