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LiteFit USA Recalled- Health Hazard

Demetria Ratchford2 years ago

Bacai Inc. has recently recalled LiteFit USA herbal diet supplements due to a health hazard.

About the LiteFit USA recall

According the Food and Drug Administration (FDA), the dietary supplements contained sibutramine which can pose a threat to consumers. Sibutramine is known to increase blood pressure and/or pulse rate in some people.

It can also pose risk for people with history of coronary artery disease, congestive heart failure, arrhythmias, or stroke. FDA recommends consumers/distributors/retailers should stop using LiteFit USA and return it to the place of purchase.

Description of LiteFit USA Recall

  • The health diet supplements are packaged in plastic bottles of 30 softgels.
  • The affected LiteFit USA lot includes the following lot number: 13165 which expires May 20th, 2017.
  • LiteFit USA was distributed worldwide to wholesalers, retailers, and through the Internet.
  • The recall involves all LiteFit USA distributed by Bacai Inc. from June 26th, 2013 to March 27th, 2014. 


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