One of the benefits of interventional cardiology fellowship training is the exposure to new technology. Two newly approved devices—the CardioMems heart failure monitoring system (St Jude Medical) and ...

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 ...

May 8 (Reuters) - 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 ...

Getinge is recalling the Cardiohelp System emergency drive over concern that it can become stuck or hard to turn due to friction being generated in the handle attachment, according to a medical device ...

Medical device maker Getinge is recalling 41 of its Cardiohelp Emergency Drive life support machines due to the risk of the device’s emergency drive becoming stuck when clinicians attempt to activate ...

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 ...

WAYNE, N.J., April 28, 2011 /PRNewswire/ -- MAQUET Cardiovascular today announced that the U.S. Food and Drug Administration has granted the company 510(k) clearance to market its CARDIOHELP System in ...

Please provide your email address to receive an email when new articles are posted on . The FDA designated the recall of Getinge’s heart-lung machine emergency drive as class I, the most serious type.

SIOUX CITY | A new machine will give the hearts and lungs of patients in critical condition at Mercy Medical Center the support needed to rest and recover. The hospital purchased a $100,000 Cardiohelp ...

SIOUX CITY | Mercy Medical Center purchased a $100,000 Cardiohelp system in December to give the hearts and lungs of patients in critical condition the support needed to rest and recover. This ...

Blessing of technology for patients suffering from oxygen shortage during surgery Sharjah: It’s a blessing of technology for all patients who are suffering from complication due to an oxygen shortage ...

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 ...