Image Prostate cancer is the most common cancer among men and the second most common cause of cancer-related deaths among American men. African-American men are more likely to get prostate cancer and twice as likely to die from the disease. The prostate is part of the male reproductive system that makes semen. The walnut-sized gland…
QMART Issues Voluntary Nationwide Recall of IMPERIAL Gold 2000, PremierZEN Extreme 3000, BURRO en PRIMAVERA 60000 & IMPERIAL Platinum 2000 Due to Presence of Undeclared Sildenafil and/or Tadalafil
Summary Company Announcement Date: March 31, 2021 FDA Publish Date: April 05, 2021 Product Type: Drugs Reason for Announcement: Recall Reason Description Undeclared Sildenafil and/or Tadalafil Company Name: QMART Brand Name: Brand Name(s) IMPERIAL Gold 2000, PremierZEN Extreme 3000, BURRO en PRIMAVERA 60000 & IMPERIAL Platinum 2000 Product Description: Product Description Dietary Supplement for male…
Ummzy LLC Issues Voluntary Nationwide Recall of Thumbs up 7 Red 70K, Shogun-X 15000mg, and Krazy Night Due to the Presence of Undeclared Tadalafil Sildenafil & Vardenafil
Summary Company Announcement Date: March 30, 2021 FDA Publish Date: March 31, 2021 Product Type: Drugs Reason for Announcement: Recall Reason Description Undeclared Sildenafil, Tadalafil, Vardenafil Company Name: Ummzy LLC Brand Name: Brand Name(s) Thumbs Up 7, Shogun, Krazy Night Product Description: Product Description Dietary Supplement for male sexual enhancement Company Announcement Palisades Park, NJ,…
Apotex Corp. Issues Voluntary Nationwide Recall of Guanfacine Extended-Release Tablets 2mg Due to Trace Amounts of Quetiapine Fumarate
Summary Company Announcement Date: March 31, 2021 FDA Publish Date: March 31, 2021 Product Type: Drugs Reason for Announcement: Recall Reason Description Trace amounts of Quetiapine Fumarate Company Name: Apotex Corp. Brand Name: Brand Name(s) Apotex Corp. Product Description: Product Description Guanfacine Extended-Release Tablets 2mg Company Announcement Weston, Florida, Apotex Corp is voluntarily recalling three…
A-S Medication Solutions Issues Voluntary Nationwide Recall of Acetaminophen Extra Strength Tablets Contained in Health Essentials Kits Due to Mislabeling
Summary Company Announcement Date: April 02, 2021 FDA Publish Date: April 02, 2021 Product Type: Drugs Reason for Announcement: Recall Reason Description Products contain an incomplete prescription drug label Company Name: A-S Medication Solutions, LLM Brand Name: Brand Name(s) A-S Medication Solutions, LLM Product Description: Product Description Acetaminophen Extra Strength 500 mg Tablets, 100 ct….
Nuri Trading LLC Issues Voluntary Nationwide Recall of Shogun-X 7000, Thumbs Up 7 (Black) 25K, Thumbs Up 7 (White) 11K, 69MODE Blue 69, Due to the Presence of Undeclared Tadalafil, Sildenafil, and/ or Vardenafil
Summary Company Announcement Date: March 29, 2021 FDA Publish Date: March 31, 2021 Product Type: Drugs Reason for Announcement: Recall Reason Description Undeclared Sildenafil, Tadalafil, Vardenafil Company Name: Nuri Trading LLC Brand Name: Brand Name(s) Thumbs Up 7, Shogun-X, 69MODE Product Description: Product Description Dietary Supplement for male sexual enhancement Company Announcement Nuri Trading is…
Infections Associated with Reprocessed Urological Endoscopes – Letter to Health Care Providers
April 1, 2021 The U.S. Food and Drug Administration (FDA) wants to raise awareness among health care providers, including those working in reprocessing units in health care facilities, about the risk of infections associated with reprocessed urological endoscopes, including cystoscopes, ureteroscopes, and cystourethroscopes, used for viewing and accessing the urinary tract. The FDA has received…
Acellular Dermal Matrix (ADM) Products Used in Implant-Based Breast Reconstruction Differ in Complication Rates: FDA Safety Communication
Date Issued: March 31, 2021 The U.S. Food and Drug Administration (FDA) is informing patients, caregivers, and health care providers that certain acellular dermal matrix (ADM) products used in implant-based breast reconstruction may have a higher chance for complications or problems. There are several methods for reconstructing the breast following mastectomy (surgical removal of the…
Mammography Problems at Tennessee Women’s Care P.C. in Nashville, TN: FDA Safety Communication
Date Issued: March 30, 2021 The U.S. Food and Drug Administration (FDA) is alerting patients who had mammograms at Tennessee Women’s Care P.C., located in Nashville, Tennessee, on or after November 1, 2019, about possible problems with the quality of their mammograms. Recommendations for Patients and Caregivers If you have had a more recent mammogram…
Antoto-K Issues Voluntary Nationwide Recall of Thumbs Up 7 Red 70K Due to the Presence of Undeclared Sildenafil and Tadalafil
Summary Company Announcement Date: March 26, 2021 FDA Publish Date: March 29, 2021 Product Type: Drugs Reason for Announcement: Recall Reason Description Undeclared Sildenafil and Tadalafil Company Name: Antoto-K Brand Name: Brand Name(s) Thumbs Up 7 Product Description: Product Description Dietary Supplement for male sexual enhancement Company Announcement Manassas, VA, Antoto-K is voluntarily recalling all…