Despite a healthy lifestyle, a full-body MRI revealed her splenic artery aneurysm. Blackburn's proactive approach led to successful surgery, emphasizing early detection and intervention's ...

Medtronic's recall of embolization device has been classified most serious by the U.S. Food and Drug Administration (USFDA), citing potential risks of severe injury or death. This decision follows the ...

In this study, to elucidate the underlying mechanisms, we employed transcriptomic analysis, which revealed a strong association between EPO-induced splenomegaly and immunosuppression of the spleen.

Bengaluru: The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as "most serious", following reports of the deaths of four patients.

Prostate artery embolization (PAE) is a procedure that helps treat urinary symptoms of an enlarged prostate without a risk of sexual side effects. Generally, both Original Medicare (parts A and B ...

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 ...

FDA Classifies Recall of Medtronic Embolization Devices as 'Most Serious' (Reuters) -The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as ...

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 ...