SAN JOSE, Calif., April 14 /PRNewswire/ -- MAQUET Cardiovascular LLC today announced the launch of HEARTSTRING III Proximal Seal System for coronary artery bypass surgery procedures. This latest ...
Getinge has recalled nearly 8,800 heart devices after receiving more than 100 complaints about them, including one report of a patient death. The recall—which began in December and came though the ...
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) ...
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 the ...
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 ...
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 they ...
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