In the United States, the device is being used under an Investigational Device Exemption (IDE) from the US Food and Drug Administration (FDA). Findings from the WAVE ... the rights of other parties; ...
Akebia Therapeutics®, Inc. (Nasdaq: AKBA), a biopharmaceutical company with the purpose to better the lives of people ...
As someone that has been covering recalls for EatingWell since 2022, I will say recalls are more common than you may think.
The maker of a homeopathic nasal spray with a history of contamination is refusing to recall its product after the Food and ...
FDA drug alerts in pulmonology, including drug approvals/warnings, vaccine approvals, medical device recalls/updates, and ...
The products were voluntarily recalled "due to the potential presence of soft plastic film," leading them to be given a Class II risk level.
Reser's Fine Foods, Inc, based in Kansas, issued a recall in August for Walmart's Freshness Guaranteed Original Macaroni Salad because of foreign material in the product, according to the FDA.
Good morning. I’m David Hilzenrath, a D.C.-based reporter for KFF Health News with an interest in medical product regulation. Had an experience with a medical device that you’d like to share?
The FDA designated the ReviveRX recall a class I — the most serious level, meaning that “there is a reasonable probability that the use of or exposure to a violative product will cause serious ...
FDA issues 19 recalls in August for food, drinks The U.S. Food and Drug Administration issued 19 recalls in August for various food and beverages. While not all of them were sold in Florida ...
More than 200 cases of Kandy cantaloupe sold at retailers in five states have been recalled after the FDA warned of potential ...