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Erectile Dysfunction News (Page 2)
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FDA Medwatch Alert: Esupplementsales, LLC Issues a Nationwide Recall All Lots of Hard Dawn Due to the Presence of Undeclared Tadalafil
January 28, 2022 - Orangevale, CA, Esupplementsales, LLC is voluntarily recalling lot number 2107 of Hard Dawn Rise and Shine capsules to the consumer level. Esupplementsales, LLC was informed by...
FDA Medwatch Alert: Namoo Enterprise LLC Issues Voluntary Nationwide Recall of PremierZen Black 5000 Due to the Presence of Undeclared Sildenafil and Tadalafil
March 26, 2021 – Little Ferry, NJ, Namoo Enterprise LLC is voluntarily recalling all lots within expiry of PremierZen Black 5000 capsules to the consumer level. FDA analysis has found the product to...
FDA Medwatch Alert: Adamssecret.co Issues Voluntary Nationwide Recall of Adam’s Secret Extra Strength 1500 and 3000 Capsules Due to Presence of Undeclared Sildenafil and/or Tadalafil
February 16, 2021 – Adamssecret.co is voluntarily recalling all lots within expiry of Adam’s Secret Extra Strength 1500 and Adam’s Secret Extra Strength 3000 capsules to the consumer level. This rec...
FDA Medwatch Alert: Nature’s Rx Issues Voluntary Nationwide Recall of Silver Bullet 10 Male Enhancement Capsules due to an Undeclared PDE-5 Inhibitor Found in The Product
November 13, 2019 – Nature’s Rx is voluntarily recalling lot: 01251ZX1, Expiry Date: 11/2022 of Silver Bullet (10 Male Enhancement Capsules). This recall has been initiated after an FDA laboratory a...
FDA Medwatch Alert: Med Man Issues Voluntary Nationwide Recall of Up2 Due to Presence of Undeclared Sildenafil
November 8, 2019 – Med Man Distribution is voluntarily recalling all lots of Up2 Dietary supplement There is no other all-natural libido for men and women to the consumer level. FDA laboratory...
FDA Medwatch Alert: GL Holdings Issues Voluntary Worldwide Recall of Green Lumber Products Due to Presence of Undeclared Tadalafil
October 22, 2019 – Newport Beach, California. GL Holdings is voluntarily recalling six lots of Green Lumber 2-, 4-, and 10-capsule packages purchased on or before August 10, 2019 to the consumer...
FDA Medwatch Alert: FDA Warns Consumers to Avoid Rhino Male Enhancement Products Found at Retailers Because of Undeclared and Potentially Dangerous Drug Ingredients
The U.S. Food and Drug Administration is warning consumers not to purchase or use Rhino male enhancement products, due to a recent rise in reported health issues. Since 2007, the FDA has identified...
FDA Medwatch Alert: Vegetable Vigra by Natures Supplement: Recall - Undeclared Drug Ingredient
[Posted 09/21/2017] ISSUE: Natures Supplement, Inc. is voluntarily recalling 260 bottles of Vegetable Vigra, 200 mg capsules to the consumer level. FDA analysis found this product to be tainted with...
FDA Medwatch Alert: Super Panther 7K by Ultra Shop Supplement: Recall - Undeclared Drug Ingredients
[Posted 07/24/2017] ISSUE: Ultra Shop Supplement is voluntarily recalling Super Panther 7K capsules, (1 count blister card Lot#: RO846356 and 6 count bottle Lot RO246852 within expiry), distributed...
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...
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