The US Food and Drug Administration (FDA) has tagged a recall of Abbott’s HeartMate 3 left ventricular assist device (LVAD) as Class I, the most serious designation for a medical device.

FDA elevates cardiovascular catheter recalls from Boston Scientific, Route 92 Medical By Conor Hale May 14, 2024 12:15pm Boston Scientific Route 92 Medical cardiovascular disease Class I recall ...

After the FDA instructed healthcare facilities to avoid using two Getinge heart devices because of quality and safety concerns, the company stopped promoting the products. In a May 14 news release ...

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 ...

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 ...

STOCKHOLM--Getinge shares trade at the bottom of the Stoxx Europe 600 index after the U.S. Food and Drug Administration advised healthcare providers to move away from using the Swedish company's ...

Last week, the FDA advised providers against using Getinge’s Cardiosave intra-aortic balloon pumps and Cardiohelp cardiopulmonary bypass systems after seeing the company start 20 recalls of the ...

May 8 (Reuters) - The U.S Food and Drug Administration (FDA) on Wednesday advised healthcare facilities to move away from using Getinge's (GETIb.ST) , opens new tab heart devices in patients as ...

DOH – 華盛頓州衛生部（DOH）、美國食品和藥物管理局（FDA）以及疾病管制與預防中心（CDC）建議人們停止食用在華盛頓州 ...

The FDA is instructing healthcare facilities to avoid using two heart devices from Getinge amid concerns that the company has not adequately resolved issues that spurred a string of recalls over ...