A penis pump can help treat erectile dysfunction (ED) by using negative air pressure to increase blood flow in the penis and create an erection. Also known as a vacuum pump or vacuum erection device, ...

The Food and Drug Administration on Tuesday classified Medtronic’s recall of its Pipeline Vantage embolization devices as the most serious type of recall. The recall removed Pipeline Vantage 027 ...

While the Steer trial enrolled treatment-naïve patients, Novartis also tested the one-time intrathecal gene therapy, coded OAV101 IT, in individuals who had tried but discontinued treatment with ...

Medtronic has recalled certain Pipeline Vantage Embolization Devices with Shield Technology due to an increased risk of incomplete wall apposition and braid deformation, which could lead to stroke ...

Medtronic has recalled embolization devices collectively linked to reports of 17 injuries and four deaths, the Food and Drug Administration said Tuesday. The recall has two elements: Medtronic is ...

After bringing Zolgensma to market in 2019 as the first gene therapy for spinal muscular atrophy, Novartis is back with an intrathecal formulation intended for older patients. Six years ago, the FDA ...

Shares of Medtronic (NYSE:MDT) reached a session low on Tuesday after the U.S. Food and Drug Administration (FDA) announced a product recall involving the company’s Pipeline Vantage 027 ...

March 18 (Reuters) - The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's (MDT.N), opens new tab embolization device as "most serious", following reports of the ...

The Pipeline Vantage embolization device. [Image courtesy of Medtronic] The FDA deemed a recall of some Medtronic (NYSE: MDT) + Pipeline Vantage embolization devices serious after multiple deaths ...

Medtronic’s top ventilator executive began fielding pleas from world leaders’ representatives five years ago, as pressure from a global pandemic drove a sudden shortage of lifesaving devices ...