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.
Getinge has initiated 20 recalls related to problems with balloon pumps and cardiopulmonary bypass devices ... and heart pumps and initiated U.S. recalls of both groups of products. The FDA ...
However, the agency is concerned that fumbling with these one-use-only devices could cost precious time in an emergency. Related FDA recalls implanted heart devices linked to 14 deaths FDA urges ...
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 ...
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 ...
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 ...