Skinny Bee Diet Supplement Recall [US]

US FlagUS/Silver Spring: Skinny Bee Diet Supplement Recall [US]Love My Tru Body recalls certain batch/lots of Skinny Bee Diet Supplements due to undeclared Desmethylsibutramine, Sibutramine and/Phenolphthalein, all controlled substances. This make the recalled Supplements a new and untested drug compound, a serious health hazard. FDA: http://ht.ly/Qhau3060kDe

Direct link: http://www.fda.gov/Safety/Recalls/ucm528429.htm

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

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Dream Body Nutritional Supplement Recall [US]

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US/Silver Spring: FDA Logo BlueDream Body Weight Loss recalls all current batch/lots of Dream Body and Body Advanced Nutritional Supplements due to undeclared Sibutramine, a restricted substance that may cause serious and potential fatal side effects requiring immediate medical intervention.
FDA: http://ht.ly/TOtN302e1xW

Direct link: http://www.fda.gov/Safety/Recalls/ucm509727.htm

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

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La’ Trim Plus, Jenesis & Oasis Supplement Recall [US]

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US/Silver Spring: BeeXtreme LLC recalls certain Dietary Supplements due to undeclared Sibutramine and/or Phenolphthalein, both serious health and safety hazards. FDA: http://ht.ly/WiWcT

Direct link: http://www.fda.gov/Safety/Recalls/ucm478883.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports this recall involves all lots of La’ Trim Plus, Jenesis and Oasis brand Dietary Supplements marketed for weight loss at the consumer level, due to findings of undeclared drug ingredients including Sibutramine and/or Phenolphthalein:

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Bee Extremely Dietary Supplement Recall [US]

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US/Silver Spring: Bee Extremely Dietary Supplement Recall [US]Bee Extremely Amazed LLC recalls certain Dietary Supplements due to undeclared Sibutramine and/or Phenolphthalein, both serious health and safety hazards. CPSC: http://ht.ly/WhJzC

Direct link: http://www.fda.gov/Safety/Recalls/ucm478794.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports this recall involves various Dietary Supplements marketed for weight loss at the consumer level, due to findings of undeclared drug ingredients including Sibutramine and/or Phenolphthalein, as follows:

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Smart Lipo365 Dietary Supplement Recall [US]

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US/Silver Spring: Smart Lipo365 recalls all lots of Smart Lipo 800, 900, 950 mg capsules due undeclared sibutramine, desmethylsibutramine and phenolphthalein, all restricted and/or withdrawn drugs. FDA: http://ht.ly/W7nHM

Direct link: http://www.fda.gov/Safety/Recalls/ucm478146.htm

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

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Lipo Escultura Dietary Supplement Recall [US]

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US/Silver Spring: Lipo Escultura Supplement Recall [US]Lipo Escultura Corp. doing business as JAT Productos Naturales Corp. recalls all Lipo Escultura within expiry due to undeclared Sibutramine and Diclofenac, both controlled substances and potentially harmful ingredients. FDA: http://ht.ly/Vvqes

Direct link: http://www.fda.gov/Safety/Recalls/ucm475550.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary Supplement is subject to this recall:

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Smart Lipo365 Dietary Supplement Recall [US]

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US/Silver Spring: SmartLipo365 recalls 122 lots of Smart Lipo 800, 900, 950 mg capsules due undeclared sibutramine, desmethylsibutramine and phenolphthalein, all restricted and/or withdrawn drugs. FDA: http://ht.ly/O6sPG

Direct link: http://www.fda.gov/Safety/Recalls/ucm449741.htm

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

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Ultra ZX Weight Loss Supplement Recall [US]

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US/Silver Spring: Ultra ZX Weight Loss Supplement Recall [US]Ultra ZX Labs recalls all Ultra ZX Weight Loss Supplements due to undeclared Sibutramine and Phenolphthalein, a serious health hazard. FDA: http://ht.ly/Kazke 

Direct link: http://www.fda.gov/Safety/Recalls/ucm437517.htm

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

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Forever Beautiful Supplement Recall [US]

US FlagUS/Silver Spring: Forever Beautiful Supplement Recall [US]REFA Enterprises recalls some Forever Beautiful Dietary Supplements due to undeclared Sibutramine and Phenolphthalein, drugs that are not approved for distribution in the United States due to known seizure, heart attack, arrhythmia and stroke as well as carcinogenicity (Cancer-causing) hazards. FDA: http://ht.ly/Ezlrd

Direct link: http://www.fda.gov/Safety/Recalls/ucm423908.htm

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JaDera, Xiyouji Qingzhi Weight Loss Supplement Recall [US]

US FDA RecallUS/Silver Spring: Dolphin Intertrade Corp. recalls due to some JaDera and Xiyouji Qingzhi Weight Loss Supplements due to undeclared Sibutramine, an unapproved drug. FDA: http://ht.ly/mz4wG

Direct link: http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm359072.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports following the recalled Supplements have been found to contain undeclared Sibutramine. This drug was a previously approved controlled substance for the treatment of obesity that was removed from the US market in October 2010 for safety reasons. This makes the recalled Supplements, unapproved new drugs.

The FDA says the following drugs are subject to this recall:2210 - JaDeraSupplement

  • JaDera Weight Loss Supplement, manufactured with a lot number of 10.06.2011 with an expiration date: 09.06.2013. These Supplements were distributed from May 2011 to May 2013.
  • Xiyouji Qingzhi Weight Loss Supplement, packaged in bottles of 30 capsules of 300mg. All lots of Xiyouji Qingzhi Weight Loss Supplement are subject to this recall. The Supplements were distributed from May 2011 to May 2013.

According to the FDA, products containing Sibutramine pose a threat to consumers because Sibutramine is known to substantially increase blood 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. These products may also interact in life threatening ways with other medications a consumer may be taking.

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