Fast Facts
- PRock Marketing LLC, of Kissimmee, Fla., is recalling all lots of Fruta Planta and Reduce Weight Fruta Planta. This is a single product marketed under two brand names.
- FDA testing confirmed that Fruta Planta contains sibutramine, a drug withdrawn from the market in December 2010 for safety reasons.
- The FDA has received multiple reports of adverse events associated with the use of Fruta Planta and Reduce Weight Fruta Planta, including several cardiac events and one death.
- Consumers should stop using this product immediately and throw it away in a sealed container where children and animals cannot gain access to it. Consumers who have experienced any negative side effects should consult a health care professional as soon as possible.
What is the Problem?
PRock Marketing LLC, is voluntarily recalling all lots of Fruta Planta and Reduce Weight Fruta Planta because FDA testing determined that the product contains sibutramine. Sibutramine is a drug that was withdrawn from the market in December 2010 for safety reasons. The FDA has received multiple reports of adverse events associated with the use of Fruta Planta and Reduce Weight Fruta Planta, including several cardiac events and one death.
Sibutramine was used in combination with a reduced calorie diet and exercise to help people who are overweight lose weight and maintain their weight loss. Sibutramine is in a class of medications called appetite suppressants. It works by acting on appetite control centers in the brain to decrease appetite What are the Symptoms of Illness/Injury?
Fruta Planta and Reduce Weight Fruta Planta poses a threat to consumers because sibutramine is known to increase blood pressure and/or pulse rate in some patients and may present a serious risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke. Sibutramine may also interact in life-threatening ways with other medications a consumer may be taking.
What Do Consumers Need To Do?
Consumers should stop using this product immediately. Consumers who have experienced any negative side effects should consult a health care professional as soon as possible. PRock Marketing’s recall notice recommends that consumers throw the product away in a sealed container where children and animals cannot gain access to it or return it to the company. Consumers may reach the company at 877-225-1009 Monday through Friday from 10:00 a.m. to 4:30 p.m.
Health care professionals and patients are encouraged to report adverse events or side effects related to the use of this product to the FDA's MedWatch Safety Information and Adverse Event Reporting Program by:
- Completing and submitting the adverse report Online: www.fda.gov/MedWatch/report.htm;
