Recalls for Dietary Supplement

Fit Firm and Fabulous Issues Voluntary Nationwide Recall of Ultimate Herbal Slimcaps Due to the Presence of Undeclared Sibutramine
11/19/2015 Food Recall

Fit Firm and Fabulous is voluntarily recalling lots 05/02/2015 to 05/01/2017 of Ultimate Herbal Slimcap capsules, to the consumer level. FDA analysis has found the product to contain undeclared sibutramine. Sibutramine was a previously approved controlled substance that was removed from the U.S. market in October 2010 for safety reasons.

  • Company:
    Fit Firm
  • Problem
    Entanglement Hazard
Detox Transforms Health and Nutrition Issues Voluntary Nationwide Recall of Dietary Supplements Due to the Presence of Undeclared Drug Ingredients
02/09/2015 Food Recall

Detox Transforms Health and Nutrition, Garner, NC announced it is conducting a voluntary recall of the following dietary supplements, to the consumer level, because they contain undeclared drug ingredients making them unapproved drugs. FDA analysis found iNDiGO and BtRim Max to contain undeclared phenolphthalein.

  • Company:
    Detox Transforms Health and Nutrition
  • Problem
    Entanglement Hazard
REFA Enterprises, LLC Issues Voluntary Nationwide Recall of Forever Beautiful Bee Pollen Due to Undeclared Sibutramine and Phenolphthalein
11/19/2014 Food Recall

REFA Enterprises, LLC is voluntarily recalling one lot of each: Forever Beautiful Bee Pollen (UPC # 6333090804632), Forever Beautiful Infinity UPC # 633090804649), to the consumer level. The products have been found to contain undeclared Sibutramine or a combination of both Sibutramine and Phenolphthalein through FDA laboratory analyses.

  • Company:
    REFA Enterprises, LLC
  • Problem
    Entanglement Hazard
Solgar, Inc. Issues Voluntary Class I Recall of ABC Dophilus Powder
11/15/2014 Food Recall

Solgar, Inc., of Leonia, NJ, is voluntarily recalling ABC Dophilus Powder. The recall was initiated, out of an abundance of caution, because the product was found to contain Rhizopus oryzae, which may cause Mucormycosis.ÂÂÂThis is a rare infection that may cause health problems to consumers, particularly pre-mature infants/infants, children, and those with weakened immune systems.ÂÂÂ

  • Company:
    Solgar, Inc.
  • Problem
    Crash And Injury Hazards
Chaotic Labz Issues Voluntary Nationwide Recall of Mayhem Dietary Supplement Due to Undeclared Dexamethasone and Cyproheptadine
11/14/2014 Food Recall

Chaotic Labz, Atkins, Arkansas, is voluntarily conducting a nationwide recall of Mayhem dietary supplement capsules, Lot #CLM061114 with an expiration date of 06/2016, to the user/consumer level. Mayhem’s intended use is as a bodybuilding supplement. FDA laboratory analysis found that Mayhem Dietary Supplement contains undeclared dexamethasone, a prescription corticosteroid commonly used to treat inflammatory conditions, and cyproheptadine, a prescription antihistamine used for seasonal allergy treatment, making this an unapproved drug.

  • Company:
    Chaotic Labz
  • Problem
    Entanglement Hazard
Nova Products, Inc. Issues Voluntary Nationwide Recall of Dietary Supplements with Undeclared Active Pharmaceutical Ingredients
03/28/2014 Food Recall

Nova Products, Inc. of Aston, Pennsylvania is voluntarily recalling the following products: African Black Ant (Lot# 2006-000926), Black Ant (Lot# 2006-3627878), XZen Gold (Lot# 130310GL), ZXen Platinum (Lot# 130520PL), XZen 1200 (Lot# 13051012), XZone Gold (Lot# 131110GL), and XZone 1200 (Lot# 13071012) at the retail level. Lot numbers are identified on the back or side of each product. FDA laboratory analysis on these products has determined that they contain undeclared amounts of sildenafil and tadalafil, active ingredients of FDA-approved drugs used to treat erectile dysfunction.

  • Company:
    Nova Products, Inc.
  • Problem
    Entanglement Hazard
Pure Edge Nutrition, LLC Issues Voluntary Nationwide Recall of Bella Vi Brand Products Due to Undeclared Sibutramine and Phenolphthalein
03/26/2014 Food Recall

Toms River, NJ, Pure Edge Nutrition, LLC is voluntarily recalling one lot of each: Bella Vi Insane Bee Pollen Capsules, Bella Vi BTrim Ultimate Boost, Bella Vi BTrim Max, Bella Vi Extreme Accelerator, Bella Vi Insane Amp’d, and two lots of Bella Vi Amp’d Up to the consumer level. The products have been found to contain undeclared Sibutramine or a combination of both Sibutramine and Phenolphthalein through FDA laboratory analyses.

  • Company:
    Pure Edge Nutrition
  • Problem
    Products contain undeclared Sibutramine and/or combination of Sibutramine and Phenolphthalein
New Life Nutritional Center Issues Voluntary Nationwide Recall of Super Fat Burner, Maxi Gold and Esmeralda Dietary Supplements Due to the Presence of Undeclared Sibutramine and Phenolphthalein
03/25/2014 Food Recall

New Life Nutritional Center is recalling all lots of “Super Fat Burner capsules, Maxi Gold capsules and Esmeralda softgels” to the user level after FDA analysis revealed the products contain undeclared active pharmaceutical ingredients: sibutramine, phenolphthalein or a combination of both sibutramine and phenolphthalein.

  • Company:
    New Life Nutritional Center
  • Problem
    Entanglement Hazard
MyNicKnaxs, LLC. Issues a Voluntary Nationwide and International Recall of All Weight Loss Formulas of Reduce Weight Fruta Planta
02/13/2014 Food Recall

MyNicKnaxs, LLC., located in Florida is announcing a recall of Reduce Weight Fruta Planta because the products contain an undeclared active pharmaceutical ingredient: Phenolphthalein. The FDA lab analysis of the product found Reduce Weight Fruta Planta to contain 10.2 mg of Phenolphthalein.

  • Company:
    Planta
  • Problem
    Entanglement Hazard
Mega Slim Herbal Appetite Management Pills by YoungYou International: Recall - Presence of DMAA
01/31/2014 Medical Recall

DMAA may cause a rise in blood pressure or other cardiovascular problems such as shortness of breath, tightening in the chest or heart attack.

  • Company:
    DMAA
Human Science Foundation Issues Voluntary Nationwide Recall of Pro ArthMax Due to Undeclared Active Pharmaceutical Ingredients
01/14/2014 Food Recall

Jan 13, 2014 – Gardena, CA, Human Science Foundation is voluntarily recalling all lots of Pro ArthMax 120 count bottle, labeled and sold as a dietary supplement to the consumer level. The product has been found to contain undeclared active pharmaceutical ingredients (APIs), making it an unapproved new drug.

  • Company:
    Human Science Foundation
  • Problem
    Listeria Monocytogenes
Stone Independent Research, Inc. Issues Allergy Alert on Undeclared Milk in EnhanceRx Dietary Supplement
12/16/2013 Food Recall

Stone Independent Research, Inc. of Syracuse, NY is recalling 15,657 units of EnhanceRx, a dietary supplement, because it contains undeclared milk (whey protein). People who have an allergy to milk run the risk of serious or life-threatening allergic reaction if they consume this product.

  • Company:
    Stone Independent Research, Inc.
  • Problem
    Drowning Hazard
Stone Independent Research, Inc. Issues Allergy Alert on Undeclared Milk in One Lot of Zanocap Capsules
12/16/2013 Food Recall

Stone Independent Research, Inc. of Syracuse, NY is recalling 1,040 units of Zanocap Scientific Weight Loss 500 mg capsules because it contains undeclared milk (whey protein). People who have an allergy to milk run the risk of serious or life-threatening allergic reaction if they consume the affected product.

  • Company:
    Stone Independent Research, Inc.
  • Problem
    Drowning Hazard
IQ Formulations Issues a Voluntary Recall of HYDRAVAX Dietary Supplement Due to Possible Undeclared Ingredient
11/29/2013 Food Recall

IQ Formulations, of Sunrise, Florida is initiating a precautionary and proactive recall of all lots of its 45-capsule bottles of HYDRAVAX due to potential inclusion of an unlisted ingredient. The FDA has advised IQ Formulations that an analysis of a sample from one lot of HYDRAVAX (Lot # 2458, Exp # 07/16) revealed the presence of an undeclared ingredient – a diuretic.

  • Company:
    IQ Formulations
  • Problem
    Entanglement Hazard
Deseo Rebajar Inc. Issues Voluntary Puerto Rico Recall of Adipotrim XT Due to Underclared Fluoxetine
11/21/2013 Food Recall

Deseo Rebajar Inc., is voluntarily recalling lot #052012 of Adipotrim XT to the consumer level. The FDA laboratory analysis of this dietary supplement found to contain undeclared Fluoxetine.

  • Company:
    Deseo Rebajar Inc.
  • Problem
    Entanglement Hazard
Fossil Fuel Products, LLC, Issues Voluntary Nationwide Recall of “RezzRX” Due to Undeclared Active Ingredients
11/19/2013 Food Recall

Fossil Fuel Products, LLC, is voluntarily recalling lots QL110714A102 (20-count bottles) and QL110408B046 (single blister packs) of “RezzRX” to the consumer level.

  • Company:
    Fossil Fuel Products, LLC
  • Problem
    Entanglement Hazard
Vitality Research Labs, LLC, Issues Immediate Voluntary Nationwide Recall of "VitaliKOR Fast Acting" Marketed as a Dietary Supplement, Due to Undeclared Active Ingredients
11/14/2013 Food Recall

Vitality Research Labs, LLC, the repackager of the VitaliKOR Products, is voluntarily recalling lots K58Q and F50Q of VitaliKOR Fast Acting to the consumer level. FDA laboratory analysis on VitaliKOR has determined that this product contains undeclared Vardenafil and Tadalafil.

  • Company:
    Vitality Research Labs, LLC
  • Problem
    Entanglement Hazard
OxyElite Pro Dietary Supplements by USP Labs: Recall - Products Linked to Liver Illnesses
11/10/2013 Medical Recall

The products contained aegeline, a new dietary ingredient that lacks a history of use or other evidence of safety.

  • Company:
    OxyElite Pro
Vega Issues Voluntary Withdrawal of Vega One Nutritional Shakes and Vega Sport Performance Protein Product Due to Traces of the Antibiotic Chloramphenicol
11/09/2013 Food Recall

Sequel Naturals Inc., dba “Vega,” announced today that it has taken the precautionary measure of voluntarily withdrawing a limited quantity of its Vega One Nutritional Shakes and Sports Performance Protein products due to finding trace amounts of chloramphenicol (CAP), a naturally occurring antibiotic. Chloramphenicol is a prescription drug commonly used to treat typhoid fever and eye infections around the world. It should only be used under medical supervision.

  • Company:
    Sequel Naturals Inc., dba “Vega,”
  • Problem
    Entanglement Hazard
Creafuse Powder Grape and Creafuse Powder Fruit Punch: Recall - Contains DMAA
09/13/2013 Medical Recall

Ingestion of DMAA can elevate blood pressure and lead to cardiovascular problems.

  • Company:
    Ge Pharma
Hardmenstore.com Issues Voluntary Nationwide Recall of 72HP, Evil Root and Pro Power Max Due to Undeclared Sildenafil
08/27/2013 Food Recall

Upon request of the FDA, Hardmenstore.com is voluntarily recalling 1000 lots of 72HP, Evil Root and Pro Power Max at the consumer level. According to representatives of the FDA, 72HP, Evil Root and Pro Power Max have reportedly been found to contain amounts of the PDE-5 Inhibitor, sildenafil, which is the active ingredient in an FDA-approved drug for erectile dysfunction (ED).

  • Company:
    Hardmenstore.com
  • Problem
    Entanglement Hazard
Jack Rabbit Inc. Conducts Voluntary Nationwide Recall of Lot 2510 of Jack Rabbit Dietary Supplement Due to undeclared ingredient
08/20/2013 Food Recall

Jack Rabbit Inc. announced today that it is conducting a voluntary nationwide recall of one lot of the company's dietary supplement product sold under the following name: Jack Rabbit. The product was found to contain Sildenafil and Tadalafil.

  • Company:
    Jack Rabbit Inc.
  • Problem
    Entanglement Hazard
Herbal Give Care LLC Issues Voluntary Nationwide Recall of Esbelder Man Capsules, Esbelder Fem Capsules, and Esbelder Siloutte Capsules Vitamin Supplements Due to Potential Health Risks
08/19/2013 Food Recall

Grand Prairie, Texas, Herbal Give Care LLC is voluntarily recalling all lots of Esbelder man (30 capsules), Esbelder fem (30 capsules) and Esbelder siloutte (30 capsules) to the consumer level. The products have been found to contain undeclared Sibutramine, N-Desmethylsibutramine, and N-di-Desmethylsibutramine.

  • Company:
    Herbal Give Care LLC
  • Problem
    Entanglement Hazard
Purity First Health Products, Inc. Issues Nationwide Recall of Specific Lots of Healthy Life Chemistry B-50, Multi-Mineral and Vitamin C Products: Due to a Potential Health Risk
08/01/2013 Food Recall

July 31, 2013 - East Northport, New York, Purity First Health Products, Inc. is voluntarily recalling two lots of Healthy Life Chemistry B-50 (100 capsules), one lot of Healthy Life Chemistry Multi-Mineral (200 capsules) and all lot numbers for Healthy Life Chemistry Vitamin C (200 capsules) to the consumer/user level. The B-50 capsules were tested by the U.S. Food and Drug Administration and have been found to contain Methasterone (schedule III controlled substance) and Dimethazine.

  • Company:
    Healthy Life Chemistry Inc. dba Purity First
  • Problem
    Entanglement Hazard
Herbal Give Care LLC Issues Voluntary Nationwide Recall of Esbelin Siloutte Te and Esbelin Siloutte Vitamin Supplement Due to Potential Health Risks
07/22/2013 Food Recall

Grand Prairie, Texas, Herbal Give Care LLC is voluntarily recalling all lots of Esbelin siloutte te and Esbelin siloutte Herbal Blend with L-Carnitine (30 Capsules), to the consumer level. The products have been found to contain undeclared Sibutramine, N-Desmethylsibutramine, and N-di-Desmethylsibutramine.

  • Company:
    Herbal Give Care LLC
  • Problem
    Entanglement Hazard
Hardmenstore.com Issues Voluntary Nationwide Recall of Silver Sword and Clalis at the Request of the FDA
07/15/2013 Food Recall

Upon request of the FDA, Hardmenstore.com is voluntarily recalling 430 lots of Silver Sword and Clalis at the consumer level. According to representatives of the FDA, Silver Sword and Clalis have reportedly been found to contain amounts of PDE-5 Inhibitor Sildenafil, which could cause adverse reactions and drug interactions normally associated with the active ingredient in Viagra.

  • Company:
    Hardmenstore.com
  • Problem
    Entanglement Hazard
Oxyphen, Phentalene, Phen FX, and Red Vipers by Beta Labs, LTD: Recall - Contains DMAA
06/24/2013 Medical Recall

Ingestion of DMAA can elevate blood pressure and lead to cardiovascular problems.

  • Company:
    DMAA