Robitussin cough syrups recalled due to 'microbial contamination,' maker says
Recall on Robitussin cough syrup announced Wednesday through FDA
Bottles of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult are being recalled due to "microbial contamination," maker Haleon announced Wednesday via the U.S. Food and Drug Administration (FDA).
Use of the affected product could potentially result in "severe or life-threatening adverse events such as fungemia or disseminated fungal infection" in immunocompromised individuals, the public health agency said in a release.
Non-immunocompromised consumers are not as likely to be exposed to health risks as a result of using the impacted products, but "the occurrence of an infection that may necessitate medical intervention cannot be completely ruled out."
The over-the-counter cough syrups are meant to be used for the temporary relief of cold, flu, hay fever and other respiratory allergy symptoms.
CDC EXPANDING TAINTED CHARCUTERIE MEAT PROBE AFFECTING COSTCO, SAM'S CLUB
Eight lots of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult have been recalled. (U.S. Food and Drug Administration)
Impacted bottles are four and eight ounces in size. Effected lot numbers and expiry dates can be found here.
Haleon, a British consumer healthcare company, told FOX Business in a statement that "a root cause has been identified and we are implementing corrective and preventative actions to ensure that this does not recur."
POSSIBLE LISTERIA CONTAMINATION PROMPTS BRIGHTFARMS SPINACH, SALAD KIT RECALL
The FDA showcases where to find the lot number and expiration date on the impacted bottles of recalled Robitussin. (U.S. Food and Drug Administration)
The company says it is notifying distributors and costumers with instructions for the return of the recalled products. Consumers who have purchased the products included in the recall should stop consumption immediately.
Anyone who believes they have experienced health problems related to taking or using the cough syrups in the recall is urged to contact their physician or healthcare provider, as well as file a report with the FDA's MedWatch Adverse Event Reporting program.
Cough syrup poured onto spoon, close-up. (Universal Images Group via Getty Images)
CLICK HERE TO READ MORE ON FOX BUSINESS
Consumers with questions can contact Haleon's Consumer Relations team at +1-800-245-1040 (Monday through Friday, 8 a.m. to 6 p.m. ET) or reach out via email to mystory.us@haleon.com.