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Erectile Dysfunction News (Page 2)
Related terms: Erection Problems, Impotence, Sexual Dysfunction, Male, ED, Impotency
FDA Medwatch Alert: Edex (alprostadil for injection) 10 mcg 2 Pack by Endo Pharmaceuticals: Recall - Potential Lack of Sterility Assurance
ISSUE: Endo Pharmaceuticals Inc. is recalling one lot of Edex (alprostadil for injection) 10 mcg to the consumer level. This product recall is due to the detection by Endo of a defect in the crimp...
FDA Medwatch Alert: Megajex Natural Male Sex Enhancer by MS Bionic: Recall - Undeclared Drug Ingredients
[Posted 12/01/2016] ISSUE: MS Bionic, Inc. announced today that it is conducting a voluntary nationwide recall of all lots of Megajex Natural Male Sex Enhancer capsules. FDA analysis has found the...
FDA Medwatch Alert: SexVoltz, Velextra, and Amerect by Beomonstar Products: Recall - Undeclared Drug Ingredient
ISSUE: BeaMonstar Products notified the public that it is recalling its SexVoltz, Velextra, and Amerect capsules to the retail level. Laboratory analysis conducted by the FDA on SexVoltz and Velextra...
FDA Medwatch Alert: Bullet Proof: Public Notification - Undeclared Drug Ingredient
ISSUE: FDA is advising consumers not to purchase or use “Bullet Proof,” a product promoted and sold for sexual enhancement on various websites and in some retail stores. FDA laboratory analysis con...
FDA Medwatch Alert: Lightning Rod Capsules: Recall - Undeclared Drug Ingredient
ISSUE: Chang Kwung announced today that it is conducting a voluntary nationwide recall of the company’s dietary supplements sold under the brand name Lightning Rod (500 mg per capsule packaged in 3...
FDA Medwatch Alert: American Lifestyle Vicerex and Black Ant Capsules: Recall - Undeclared Drug Ingredient
ISSUE: May 1, 2013 - American Lifestyle is announcing that it is conducting a voluntary recall of all lots of Vicerex UPC 893490820087 and Black Ant UPC 4026666142546. Laboratory analysis conducted...
FDA Medwatch Alert: Affirm XL Recall - Undeclared Drug Ingredient
ISSUE: Affirm XL, Inc. is conducting a voluntary recall to the consumer level after FDA lab analysis testing found the product to contain an analogue of sildenafil. Sildenafil is an active ingredient...
FDA Medwatch Alert: ROCK-It MAN Male Enhancement Capsules: Recall - Undeclared Drug Ingredient
ISSUE: Consumer Concepts, Inc. notified the public of a consumer/user level recall of all ROCK-It MAN Male Enhancement Capsules sold between October, 2012 and April, 2013. Analytical tests conducted...
FDA Medwatch Alert: Palimed Solutions, Inc. Sterile Compound Products: Recall - Visible Particulates Observed
ISSUE: Pallimed Solutions, Inc. of Woburn, MA, doing business as Pallimed Pharmacy, is voluntarily recalling all sterile compound products dispensed since January 1, 2013 to the user level, including...
FDA Medwatch Alert: Night Bullet: Recall - Undeclared Drug Ingredient
ISSUE: Green Planet, Inc. notified the public of a recall of its dietary supplement product Night Bullet. Analytical tests conducted by the FDA found that the product contains trace amounts of...
FDA Medwatch Alert: Libigrow, Libigrow XXXtreme, Blue Diamond, Blue Diamond Platinum, Mojo Nights, Mojo Nights Supreme, And Casanova: Recall - Undeclared Ingredients Sulfoaildenafil and Thioaildenafil
[Posted 12/18/2012] ISSUE: Performance Plus Marketing, Inc. Issues a Voluntary Nationwide Recall of Libigrow, Libigrow XXXtreme, Blue Diamond, Blue Diamond Platinum, Mojo Nights, Mojo Nights...
FDA Medwatch Alert: Mojo Nights and Mojo Nights for Her: Recall - Undeclared Drug Ingredient
ISSUE: Evol Nutrition Associates, Inc./Red Dawn (“Evol Nutrition”) notified the public of a nationwide recall of all lots of two dietary supplement products distributed by the company under the names ...
FDA Medwatch Alert: V Maxx RX: Recall - Undeclared Drug Ingredient
ISSUE: The Menz Club, LLC issued a nationwide recall of V Maxx Rx due to undeclared sulfoaildenafil. Sulfoaidenafil is an analog of sildenafil, an FDA approved prescription drug used to treat...
FDA Approves Stendra for Erectile Dysfunction
April 27, 2012 – The U.S. Food and Drug Administration today approved Stendra (avanafil), a new drug to treat erectile dysfunction. Erectile dysfunction is when a man has trouble getting or keeping...
FDA Medwatch Alert: X-Rock: Recall - Undeclared Drug Ingredient
ISSUE: X-Rock Industries LLC is conducting a recall of certain supplement products under the brand name of X-ROCK. Analytical tests of X-ROCK for Men conducted by FDA concluded that the products...