The U.S. Food and Drug Administration classified a recall of Teleflex's inflatable devices that increase blood supply to the ...
The FDA says a recall of Teleflex (NYSE:TFX) intra-aortic balloon catheter kits is Class I, the most serious kind of recall.
The FDA recently labeled a recall of Abbott (NYSE: ABT) + Abbott Laboratories $105.79 1.58% Open 107.32 Day High 107.32 52 ...
Heart failure (HF) is a significant factor driving the growth of mechanical circulatory support devices (MCSDs), which are used in three therapies for patients not eligible for heart transplants ...
The US Food and Drug Administration (FDA) has tagged a recall of Abbott’s HeartMate 3 left ventricular assist device (LVAD) as Class I, the most serious designation for a medical device.
FDA reports 322 complaints, 31 injuries and 3 deaths related to Teleflex and Arrow International's intra-aortic balloon pumps. Learn more about the recall here.
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 ...
May 22 (Reuters) - The U.S. Food and Drug Administration on Wednesday classified a recall of Hologic's (HOLX.O) , opens new tab devices that are implanted in soft tissue such as breast tissue as ...
Several cases of yogurt-covered pretzels have been recalled due to fears they could be contaminated with salmonella. A recall ...