The Food and Drug Administration in a letter Wednesday told healthcare providers and facilities they should stop using certain Getinge cardiovascular medical devices. Getinge has initiated 20 recalls ...

Add Yahoo as a preferred source to see more of our stories on Google. FILE PHOTO: Signage is seen outside of the Food and Drug Administration (FDA) headquarters in White Oak, Maryland, U.S. (Reuters) ...

Several years into the process of rectifying potential breaches in the sterile packaging of its life support systems—a process that has been littered with field correction notices and FDA-rated ...

Getinge said Tuesday it has paused promotional activities of certain balloon pumps and cardiopulmonary bypass devices in the U.S. The company, which is limiting sales to customers that lack ...

Certain cardiovascular devices made by Getinge/Maquet remain problematic and should be avoided if possible, the US Food and Drug Administration said Wednesday in a letter to healthcare providers. The ...

The warning covers Getinge/Maquet/Datascope Cardiosave Hybrid and Rescue Intra-Aortic Balloon Pump (IABP) devices and the Getinge/Maquet Cardiohelp system and HLS sets Physicians are in short supply.

London: The U.S Food and Drug Administration (FDA) on Wednesday advised healthcare facilities to move away from using Getinge's heart devices in patients as they faced safety and quality concerns ...