May 8 (Reuters) - The U.S Food and Drug Administration (FDA ... opens new tab heart devices in patients as they faced safety and quality concerns despite a string of recalls.
May 8 (Reuters) - The U.S Food and Drug Administration (FDA ... using Getinge's heart devices in patients as they faced safety and quality concerns despite a string of recalls.
In a statement Wednesday, the FDA said it recommended providers find alternatives to Getinge's balloon pump and bypass devices ... to the heart's left ventricle. Eight of the recalls fall within ...
In a statement Wednesday, the FDA said it recommended providers find alternatives to Getinge's balloon pump and bypass devices ... to the heart's left ventricle. Eight of the recalls fall within ...
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 ...
London: The U.S Food and Drug Administration (FDA ... from using Getinge's heart devices in patients as they faced safety and quality concerns despite a string of recalls. The recommendation ...
“The FDA recommends that health care facilities transition away from use of these devices and ... Getinge heart balloon pumps further deflated by 4 more Class I recalls and 6 reported patient ...
After the FDA instructed healthcare facilities to avoid using two Getinge heart devices because of quality ... After numerous recalls and corrections, the FDA said it is still receiving reports ...
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 ...
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 ...
the FDA said. The problem impacts the integrity of the blood flow and may lead to longer-than-expected surgery, hemorrhage, right heart failure or air embolism. The agency said 882 devices ...
Getinge has initiated 20 recalls related to problems with balloon pumps and cardiopulmonary bypass devices in less than 16 months, according to the notice. The FDA is concerned Getinge has yet to ...