After the FDA instructed healthcare facilities to avoid using two Getinge heart devices because of quality and safety concerns, the company stopped promoting the products. In a May 14 news release ...
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 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 ...
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 ...
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 ...
Initiated by Abbott/Thoratec and deemed Class I by the FDA, the recall is in response to reports of 70 injuries and two ...
STOCKHOLM--Getinge shares trade at the bottom of the Stoxx Europe 600 index after the U.S. Food and Drug Administration advised healthcare providers to move away from using the Swedish company's ...
Getinge said Tuesday it has paused promotional activities of certain balloon pumps and cardiopulmonary bypass devices in the U.S. The company, which is limiting sales to customers that lack ...
Masimo recently announced the recall of some of its Rad-G pulse oximeters after reports of unintended change of device power state. Nabbing FDA clearance in September 2020, Rad-G is a portable SET ...
In the latest notice, which follows a February recall of the device for a separate issue, Abbott took action due to reports of blood leakage and air entrapment.