LiteFit USA Herbal Diet Supplement Recall [US]

USDA Recall

US/Silver Spring: 3451 - LiteFitHerbalDietSupplementBacai recalls some LiteFit USA HerbalDiet Supplements due to the presence of Sibutramine, a controlled drug. FDA:

Direct link:

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Herbal Diet Supplements are subject to this recall:

  • LiteFit USA Herbal Diet Supplement, lot number 13165; expires: May 2017. LiteFit USA was distributed worldwide to wholesalers, retailers and through the Web.

Additional information:
According to the FDA, Sibutramine is a controlled substance that was removed from the US market in October 2010 for safety reasons. The Herbal Diet Supplement poses a threat to consumers because Sibutramine is known to substantially increase recalled pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of Coronary Artery Disease, Congestive Heart Failure, Arrhythmias or Stroke. This Supplement may also interact, in life-threatening ways, with other medications a consumer may be taking.


Recalls Direct RIN: 3451-2014
About the Recalls Direct service:
Visit the Living Safely site:
E. & O.E.

☞ Want to e-mail or share this recall? Simply use the “Share this” options below.
☞ Is this recall relevant to you? Click on the “Like this” button below.

%d bloggers like this: