On Wednesday April 1, the US Food and Drug Administration (FDA) ordered that Zantac be pulled from the market. Zantac is a well-known drug used to...
The new drug from Gilead Sciences Inc., Descovy, has been approved by the US Food and Drug Administration for the use to reduce the risk of...
The US Food and Drug Administration is warning patients using Medtronic defibrillators and home monitors that their devices are vulnerable to cybersecurity issues and could be...
The FDA has highlighted a recent medical recall of transseptal needles, designating it as a Class I recall—the most serious level of recall. The transseptal needles...
The US Food and Drug Administration recently warned about the risks associated with using robotic devices during mastectomies and other cancer surgeries. The agency is cautioning...
The US Food and Drug Administration has issued yet another warning regarding the recall of the LifeVest 4000, after two patients died in relation to these...
The U.S. Food and Drug Administration has just flagged a common medical device—surgical staplers and implantable staples—because of a heightened risk associated with their use in...
The U.S. Food and Drug Administration is updating its warning about surgical balloons and stents that are coated in the drug paclitaxel. The agency’s letter warns...
The U.S. Food and Drug Administration has issued a report warning the public about the risks of the drug tofacitinib. A recent clinical trial determined that...
The U.S. Food and Drug Administration recently warned that a common gout prescription may increase your chances of death from heart-related issues. The drug is Uloric...
