Alerts and Advisories

• Actra-Rx (11/02/2004)
• Androstenedione (Andro): FDA Warning (03/11/2004)
• Aspire36 and Aspire Lite Recalled, Palo Alto Labs Issues a Voluntary Nationwide Recall of two Products Marketed as Dietary Supplements (FDA; 02/28/2008)
• Atlas Operations, Inc. Announces Expansion of its Nationwide Voluntary Recall of Specific Lots of Sexual Enhancement Products Marketed as Dietary Supplements (FDA; 04/12/2010)
• Atlas Operations, Inc. Recalls Many Sexual Enhancement Products (FDA; 12/15/2009)
• Ayurvedic Products Caution (FDA; 10/16/2004)
• Bismacine Not Approved For Use (FDA; 07/21/2006)
• Bodybuilding.com and FDA Recall 65 Products (FDA; 11/03/2009)
• Body Building Products Marketed as Containing Steroids or Steroid-Like Substances: FDA Public Health Advisory (FDA; 07/28/2009)
• Cautions about Sexual Enhancement Products (FDA; 03/08/2010)
• Consumers Warned Not to Use "Blue Steel" and "Hero" Products (FDA; 03/25/2008)
• Coral Calcium (01/22/2004)
• Don't Get Burned: Stay Away From Ear Candles (FDA; 02/18/2010)
• Ear Candles: Ineffective and Risky (FDA Patient Safety News video)
• Ejaculoid XXTREME (Nutraloid Lab) Recalled: Undeclared Drug Ingredient (FDA; 07/30/2010)
• 'Energy Max,' 'True Man Sexual Energy' Recall (FDA; 11/02/2007)
• Ephedra Consumer Advisory (04/12/2004)
• FDA, FTC Issue Joint Warning Letter to Web Site Offering Fraudulent H1N1 Flu Supplements (FDA; 10/19/2009)
• Fraud Awareness (FDA)
• Fraudulent Flu Products Warnings (FDA; 05/01/2009)
• Garlic Supplements Can Impede HIV Medication (NIH; 12/05/2001)
• Green Tea for Certain Cancers: FDA Review (FDA; 06/30/2005)
• Herbal Science International, Inc. Recalls Twelve Dietary Herbal Supplements Nationwide Because of Possible Health Risk Associated with Ephedra, Aristolochic Acid and Human Placenta (FDA; 04/10/2007)
• High-Strength Hydrogen Peroxide Causes Serious Harm (FDA; 07/27/2006)
• Hydroxycut, FDA Warns Consumers to Stop Using These Products (FDA; 05/01/2009)
• IDS Sports Voluntary Nationwide Recall of Products (FDA; 11/12/2009)
• Jen-On's H S Joy of Love Product Recall (FDA; 04/17/2007)
• Joyful Slim Herb Supplement Recalled: Undeclared Drug Ingredient (FDA; 07/22/2010)
• Libipower Plus Recall (FDA; 07/13/2009)
• Liquid "Energy" Product Warning (FDA; 07/07/2009)
• "Litargirio" Powder Contains Dangerous Lead Levels (FDA; 10/02/2003)
• Long Weekend Product Recalled Nationwide (FDA; 06/14/2007)
• Liviro3 Voluntary Nationwide Recall (FDA; 01/19/2007)
• Magic Power Coffee Warning (FDA; 06/19/2010)
• Marketers of Acai Berry Supplements and "Colon Cleansers" Ordered to Halt Sales (FTC; 08/16/2010)
• MasXtreme Capsules (Natural Wellness)—Product Contains Undeclared Drug Ingredient (FDA; 03/30/2010)
• Miracle Mineral Solution (MMS): Product As Consumed Produces a Potent Bleach (FDA; 07/30/2010)
• Mr. Magic Male Enhancer: Undeclared Drug Ingredient (FDA; 08/18/2010)
• Nature and Health Co. Recalls Supplement Products (FDA; 07/15/2009)
• Novacare LLC Conducts Voluntary Nationwide Recall of Products Found to Contain Undeclared Drug Ingredient (FDA; 08/10/2010)
• Nzu, Traditional Remedy for Morning Sickness (FDA; 12/31/2009)
• Pai You Guo, Marketed as Dietary Supplement, Recalled (FDA; 11/13/2009)
• PC SPES and SPES Dietary Supplements (09/05/2002)
• Prolatis’: Undeclared Drug Ingredient (FDA; 08/13/2010)
• Que She Herbal Supplement Sold for Weight Loss: Undeclared Drug Ingredients (FDA; 07/08/2010)
• Red Yeast Rice and Red Yeast Rice/Policosonal Complex Products and Cholestrix Product Warning (FDA; 08/09/2007)
• Revivexxx Extra Strength (EZVille, Ltd.) Recalled: Undeclared Drug Ingredient (FDA; 08/06/2010)
• Rize 2 The Occasion Capsules and Rose 4 Her Capsules Voluntary Nationwide Recall (FDA; 07/28/2008)
• RockHard Weekend Recalled: Undeclared Drug Ingredient (FDA; 11/18/2009)
• Sexual Enhancement: Dangerous Dietary Supplements (07/12/2006)
• Shark Cartilage Capsules, Action Labs Inc., have Possible Health Risk (FDA; 06/06/2007)
• Shark Cartilage Capsules, NBTY, Nationwide Product Recall (FDA; 05/26/2007)
• Slim-30 Herb Weight Loss Supplement Contains Undeclared Drug (FDA; 07/16/2010)
• Solo Slim (EZVille, Ltd.) Recalled: Undeclared Drug Ingredient (FDA; 08/06/2010)
• Stamina-Rx Dietary Supplement Products (06/19/2009)
• Starcaps Dietary Supplement Capsules Recalled (FDA; 12/08/2008)
• Steam Dietary Supplement (FDA)
• Steroids or Steroid-Like Substances Marketed in Body Building Products: FDA Public Health Advisory (FDA; 07/28/2009)
• Stealth Chocolate, Stealth Vanilla Powdered Dietary Supplement Recall (FDA; 07/09/2009)
• Stimuloid II (Nutraloid Lab) Recalled: Undeclared Drug Ingredient (FDA; 07/30/2010)
• TimeOut Capsules Contaminated With Potentially Dangerous Ingredient (FDA; 08/25/2010)
• "Total Body Formula" and "Total Body Mega Formula" Consumer Warning (FDA; 03/27/2008)
• 'True Man Sexual Energy,' 'Energy Max' Recall (FDA; 11/02/2007)
• Weight Loss, FDA Uncovers Additional Tainted Products (FDA; 03/20/2009)
• Vialipro Dietary Supplement Recalled: Undeclared Drug Ingredient (FDA; 07/20/2010)
• Viapro 375 mg Capsules Voluntary Nationwide Recall by EG Labs (FDA; 07/23/2008)
• Vinarol and Viga Tablets Contaminated with Sildenafil (Viagra) (06/06/2003)
• Viril-Ity-Power (VIP) Tabs Recalled by International Pharmaceuticals (FDA; 05/29/2008)
• Vita Breath Supplement Contains High Levels of Lead (FDA; 05/03/2010)
• Vitamin D Liquid, Infant Overdose Risk (FDA; 06/15/2010)
• Vitamin E Supplements (10/28/2008)
• Vitamin Supplementation To Prevent Cancer and Cardiovascular Disease (AHRQ; Jun 2003)
• Young You Weight Loss Products Recalled (FDA; 07/15/2009)
• Zencore Plus, a Product Marketed as a Dietary Supplement, Voluntary Recalled Nationwide by Bodee LLC (FDA; 03/11/2009)
• Zicam Cold Remedy Nasal Products—Warnings (FDA; 06/16/2009)