LiteFit USA Recalled- Health Hazard
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.