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: http://ht.ly/wrS0U

Direct link: http://www.fda.gov/Safety/Recalls/ucm395538.htm

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

Herbal Give Care Esbelder Recall [US]

US FDA RecallUS/Silver Spring: Herbal Give Care recalls all lots of Esbelder man (30 capsules), Esbelder fem (30 capsules) and Esbelder siloutte (30 capsules) Nutritional Supplements due to undeclared drug hazard. FDA: http://ht.ly/o8dhO 

Direct link: http://www.fda.gov/Safety/Recalls/ucm365487.htm

Additional information:2420 - HerbalGiveCareEsbelder
The US Food and Drug Administration (“FDA”) reports the following Nutritional Supplements are subject to this recall:

  • Esbelder fem (30 capsules) is packaged in a white plastic bottle with a screw cap containing 30 capsules per bottle. All lots of this product are being recalled. The product was distributed nationwide to retail customers and via the Web. The UPC code for this product is 7502011000251.
  • Esbelder man (30 capsules) is packaged in a white plastic bottle with a screw cap containing 30 capsules per bottle. The product was distributed nationwide to retail customers and via the Web. The UPC code for this product is 7502011000275.
  • Esbelder Siloutte (30 capsules) is packaged in a white plastic bottle with a screw cap containing 30 capsules per bottle. The product was distributed nationwide to retail customers and via Web. The UPC code for this product is 7502011000268.

According to the FDA, the recalled Nutritional Supplements have been found to contain undeclared Sibutramine, N-Desmethylsibutramine and N-di-Desmethylsibutramine. The presence of these undeclared ingredients makes these products unapproved drugs. These Supplements may 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.

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Recalls Direct RIN: 2013-2420
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Bethel Advance, Quick Thin Supplement Recall [US]

US FDA RecallUS/Silver Spring: Bethel Nutritional Consulting expands an existing recall for some Bethel Advance and Quick Thin Nutritional Supplements due to undeclared drug ingredient hazard. FDA: http://ht.ly/nGgz0

Direct link: http://www.fda.gov/Safety/Recalls/ucm363939.htm

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

  • Bethel 30, bearing Lot #120514 with expiry 12/05/2014 (previously recalled);
  • Bethel Advance, bearing Lot #10092011 with expiry 2014; and
  • Quick Thin, bearing Lot #10032011 with expiry 10/2014.

According to the FDA, samples of the Quick Thin Gold Capsules and Bethel Advance White Capsules were tested and found to contain Sibutramine and Phenolphthalein. Both of these undeclared drugs may pose a threat to consumers as follows:

  • 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. This product may also interact, in life-threatening ways, with other medications a consumer may be taking. Sibutramine is a controlled substance that was removed from the US market in October 2010 for safety reasons.
  • Phenolphthalein may present health risks that could include potentially serious gastrointestinal disturbances, irregular heartbeat, muscle cramps and Cancer with long-term use. No illnesses or injuries have been reported to Bethel Nutritional Consulting to date in connection with these products.

According to Bethel Nutritional Consulting, these Supplements were sold directly to individual customers from its New York, NY, sales office and online at http://www.bethel30.com. The company has discontinued distribution and sales of these products.

Please note: other Dietary Supplements manufactured by this company have been recalled. To see all recalls and notifications related to this manufacturer, please search for “Bethel Nutritional” using the Search Box at the top of this page.

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Additional information about this recall:
Recalls Direct RIN: 2013-2356
Back to the main Recalls Direct page: http://www.RecallsDirect.com/
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Herbal Give Care Nutritional Supplement Recall [US]

US FDA RecallUS/Silver Spring: Herbal Give Care recalls some Esbelin Siloutte Nutritional Supplements due to undeclared drug hazard, specifically,  Sibutramine, N-Desmethylsibutramine and N-di-Desmethylsibutramine. FDA: http://ht.ly/ndsj2

Direct link:  http://www.fda.gov/Safety/Recalls/ucm361950.htm

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

  • Esbelin Siloutte Herbal Blend with L-Carnitine: this Supplement is marketed to help normalize nervous appetite as well as prevent fat accumulation and fluid retention in tissues. The Esbelin Siloutte Herbal Blend with L-Carnitine (30 Capsules) is packaged in a white plastic bottle with a screw cap containing 30 capsules per bottle. All lots of this product are being recalled. This Supplement was distributed nationwide to retail customers and via the internet. The UPC code for this product is 7502011000060.
  • Esbelin Siloutte Te: this Supplement is marketed as a fat burner, in that it is claimed to remove the fat stored in the body, thereby achieving elimination of the fat through the urine and preventing its accumulation. The product is also marketed to promote the proper functioning of the consumer’s digestive system. This product is packaged in a gold resealable foil pouch; the product does not have the unit size labeled. The recall includes all lots of the Esbelin Siloutte Te. This Supplement was also distributed nationwide to retail customers and via the internet. The UPC code for this product is 7562684652553.

According to the FDA, both Supplements pose dangers 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.

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Recalls Direct RIN: 2013-2297
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Bethel 30 Weight Loss Pill Recall [US]

US FDA RecallUS/Silver Spring: Bethel Nutritional Consulting recalls some Bethel 30 Weight Loss Pills due to undeclared drug hazard. FDA: http://ht.ly/lVWvk

Direct link: http://www.fda.gov/Safety/Recalls/ucm356233.htm

Additional information:
Bethel Weight Loss Front of BottleThe US Food and Drug Administration (“FDA”) reports some Bethel 30 Weight Loss Pills tested positive for Sibutramine and Phenolphthalein, two undeclared drugs. Sibutramine is a controlled substance removed from the market in October 2010 for safety reasons. The FDA has not approved Bethel 30, Green Capsules as drugs; therefore the safety and effectiveness of this product is unknown.Bethel Weight Loss Bottle Label

According to the US FDA, these products may 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. This product may also interact, in life-threatening ways, with other medications a consumer may be taking.

Please note: other Dietary Supplements manufactured by this company have been recalled. To see all recalls and notifications related to this manufacturer, please search for “Bethel Nutritional” using the Search Box at the top of this page.

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Additional information about this recall:
Recalls Direct RIN: 2013-2114
Back to the main Recalls Direct page: http://www.RecallsDirect.com/
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Bee Pollen, Nutritional Capsule Recall [US]

US/Silver Spring: Zi Xiu Tang Success recalls some Bee Pollen, Nutritional Capsules due to undeclared Sibutramine, a drug. FDA: http://ht.ly/eVGlZ

Direct link: www.fda.gov/Safety/Recalls/ucm326267.htm

Additional information:
The US Food and Drug Administration (“FDA”) says products containing Sibutramine pose a threat 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.

E. & O. E.

Healthy People Dietary Supplement Recall [US]

US/Silver Spring: Healthy People Co. expands recall for some Dietary Supplements due to undisclosed prescription drugs, specifically Sibutramine and Tadalafil. FDA: http://ht.ly/9eq7F

E. & O. E.

 

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