Categories
Plastikon Healthcare, LLC is issuing an update to the voluntary recall initiated on June 3, 2022. The recall has been expanded to include Lot 20076A of Magnesium Hydroxide 1200 mg / Aluminum Hydroxide 1200 mg / Simethicone 120 mg per 30 mL Oral Suspension. This lot was previously subject to a retai
Categories
VI-Jon, LLC Expands Voluntary Worldwide Recall of All Flavors and Lots within Expiry of Magnesium Citrate Saline Laxative Oral Solution Due to Microbial Contamination
Vi-Jon, LLC is revising a previously reported list of all flavors of Magnesium Citrate Saline Laxative Oral Solution within expiry
Categories
FDA Continues Efforts to Support Innovation in Medical Device Sterilization
FDA Continues Efforts to Support Innovation in Medical Device Sterilization
http://www.fda.gov/news-events/press-announcements/fda-continues-efforts-support-innovation-medical-device-sterilization
Categories
Loud Muscle Science, LLC Issues Voluntary Recall of Launch Sequence Capsules Due to the Presence of Undeclared Tadalafil in United States and Canada
Hauppauge, NY, Loud Muscle Science, LLC is voluntarily recalling the following Launch Sequence products and lots listed in the table below to the consumer level. Laboratory analysis undertaken at the request of Loud Muscle Science, LLC found the products to be tainted with tadalafil, an ingredient i
Categories
FDA Roundup: August 2, 2022
FDA Roundup: August 2, 2022
http://www.fda.gov/news-events/press-announcements/fda-roundup-august-2-2022
Categories
Distributor RFR, LLC, Voluntary Nationwide Recall of Sangter Energy Supplement Due to Presence of Undeclared Sildenafil
Miami, Florida, DISTRIBUTOR RFR, LLC. is voluntarily recalling lot #48656, Exp. 01/2025 of SANGTER Energy Supplement, 3000 mg, packaged in 7-count blister packs within a carton to the consumer level. FDA analysis has found the product to contain undeclared sildenafil. Sildenafil is a phosphodiestera
Categories
North American Diagnostics Recalls Oral Rapid SARS-CoV-2 Rapid Antigen Test Kits That Are Not Authorized, Cleared, or Approved by the FDA
North American Diagnostics Recalls Oral Rapid SARS-CoV-2 Rapid Antigen Test Kits because they are not authorized, cleared, or approved by the FDA.
Categories
FDA Roundup: July 29, 2022
FDA Roundup: July 29, 2022
http://www.fda.gov/news-events/press-announcements/fda-roundup-july-29-2022
Categories
FDA Infant Formula Update: July 29, 2022
FDA Infant Formula Update: July 29, 2022
http://www.fda.gov/news-events/press-announcements/fda-infant-formula-update-july-29-2022
Categories
FDA Provides Update on Agency Response to Monkeypox Outbreak
FDA Provides Update on Agency Response to Monkeypox Outbreak
http://www.fda.gov/news-events/press-announcements/fda-provides-update-agency-response-monkeypox-outbreak