STOCKHOLM, Sweden--(BUSINESS WIRE)--Regulatory News: Getinge AB, (STO:GETIB) a global medical technology company with, among other, operations in the cardiac surgery and vascular surgery markets, ...

The US Food and Drug Administration (FDA) has alerted users of Datascope Corp/MAQUET’s Cardiosave hybrid intra-aortic balloon pump (IABP) to a “design issue” that enables fluids to leak into the ...

Datascope Corp. announced today that it has mailed a letter to shareholders asking them to vote against a dissident shareholder s nominees for two board of directors slots at next week s ...

The U.S. FDA reported yet another recall of intra-aortic balloon pumps made by Datascope Corp., an unfortunate development for patients in need of these devices that are still on the FDA’s list of ...

Please provide your email address to receive an email when new articles are posted on . The FDA announced that Maquet Datascope Corp. has recalled a hybrid intra-aortic balloon pump due to a design ...

The U.S. FDA recently posted another round of recalls for the Cardiosave line of intra-aortic balloon pumps (IABPs) by Datascope Corp., advising users to make sure they have a backup unit at the ready ...

— Datascope Corp./Maquet initiated a voluntary worldwide field correction of some of its intra-aortic balloon pumps (IABPs) due to a potential mechanical failure of the fan assembly associated with ...

Datascope Corp. today announced it has inked an agreement to sell its patient monitoring business for $202 million in cash to Mindray Medical International Limited, a Shenzhen, China-based medical ...

WAYNE, N.J., June 16, 2017 /PRNewswire/ -- Datascope Corp. today announced the filing of a motion to join Maquet Cardiovascular LLC's existing patent infringement case against Abiomed, Inc. in the ...

Please provide your email address to receive an email when new articles are posted on . The FDA issued a safety alert announcing that Datascope Corp. issued a voluntary field correction for ...