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Family Doctors Find It Tough To Talk Sex With Patients
WEDNESDAY, May 14, 2025 — Sex is an important part of people’s health, but family doctors find it tougher to counsel and treat patients for sexual health matters, a new study says. General pra...
NeuroSAFE Improves Erectile Function After Radical Prostatectomy
THURSDAY, April 3, 2025 – Use of the NeuroSAFE technique, a standardized frozen section analysis that enables accurate real-time detection of positive surgical margins during nerve sparing in...
New Surgical Technique Preserves Erectile Function In Prostate Cancer Patients
FRIDAY, March 28, 2025 – A pioneering technique can help nearly twice as many men preserve erectile function following prostate cancer surgery, researchers say. The new surgical method, called...
HoLEP Double-n Technology Promising for Benign Prostatic Hyperplasia
THURSDAY, Feb. 6, 2025 – For men with benign prostatic hyperplasia (BPH), transurethral Holmium Laser of the Prostate (HoLEP) with Double-n Technology shows promise for improving urinary symptoms...
Long-Term Complications After Prostate Cancer Treatment Not Uncommon
FRIDAY, Nov. 8, 2024 – Prostate cancer (PCA) treatment is associated with increased rates of complications in the 12 years after treatment, according to a study published online Nov. 7 in JAMA...
FDA Medwatch Alert: Male Enhancement Supplements Recalled
June 11, 2024 – Integrity Products , St Louis MO is voluntarily recalling tainted lot (HGW221116) within expiry of the Ram It & To The Moon capsules to the consumer level. FDA analysis founds these...
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...