A Bunch of Robitussin Cough Syrup Was Just Recalled Due to Microbial Contamination

A Bunch of Robitussin Cough Syrup Was Just Recalled Due to Microbial Contamination

We’re in the middle of cold and influenza season– not to discuss a spike in COVID cases— so it’s most likely that you’ve just recently equipped your medication cabinet with over the counter medication to assist you deal. If your stash consists of any Robitussin, you may wish to examine your bottles: Some type of its cough syrups were simply remembered following reports of microbial contamination.

On January 24, Haleon– the business that produces Robitussin and other health items, consisting of Sensodyne and Flonase– simply remembered 8 great deals of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult, according to the Fda (FDA). These items are typically utilized to deal with typical cold and influenza signs, like coughing, fever, and aching throat.

The following 8 lots have actually been remembered– 6 are the daytime variation, and the staying 2 are the nighttime formula. Try to find the following lot numbers (which you can discover on the bottom right on the back label) on your bottles for Robitussin Honey CF Max Day Adult:

  • T10810
  • T08730
  • T08731
  • T08732
  • T08733
  • T10808

The 2 remembered lots for Robitussin Honey CF Max Nighttime Adult are T08740 and T08742.

While no cases of unfavorable results have actually been reported, it’s particularly essential for immunocompromised individuals to prevent or stop utilizing this item due to the fact that it might trigger them possibly dangerous infections, consisting of fungemia (fungis or yeast in the blood) or shared fungal infection (a term for a group of fungal infections throughout the body), per the FDAExtreme infections are not likely in non-immunocompromised individuals, it’s still an excellent concept to err on the side of care and toss these items out, according to the FDA’s statement

If you’re experiencing any adverse effects associated with making use of the above items, please contact a physician or visit your closest emergency clinic. You can likewise report any negative responses to the FDA’s MedWatch Adverse Reporting program online here

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