T wo implanted heart devices used by patients in end-stage heart failure are now under a strict U.S. Food and Drug Administration recall, after being tied to 273 known injuries and 14 deaths, the ...
Abbott’s latest HeartMate troubles are related to two deaths as well. The company initiated the recall of its HeartMate 3 ...
Two implanted heart devices used by patients in end-stage heart failure are now under a strict U.S. Food and Drug Administration recall, after being tied to 273 known injuries and 14 deaths, the ...
A pair of heart devices linked to hundreds of injuries and at least 14 deaths has received the FDA's most serious recall, the agency announced Monday. The recall comes years after surgeons say ...
Initiated by Abbott/Thoratec and deemed Class I by the FDA, the recall is in response to reports of 70 injuries and two ...
The FDA is recalling an insulin pump app. The t:connect mobile app may drain the battery of its linked insulin pump, causing ...
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.
The U.S Food and Drug Administration (FDA) on Wednesday advised healthcare facilities to move away from using Getinge's heart ...
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 heart ...
FDA Recalls Heart Failure Devices Linked to Injuries and Deaths By Ernie Mundell HealthDay Reporter WEDNESDAY, April 17, 2024 (HealthDay News) -- Two implanted heart devices used by patients in ...