The FDA classified about 1,460 Hamilton Medical ventilators in a Class I recall, part of a voluntary correction, because electrolyte fluid might leak onto the device’s control board. A leakage could ...

FDA recently announced that Hamilton Medical is recalling its Hamilton C1/T1/MR-1 ventilators. The recall is identified as Class I. The company originally sent an Urgent Medical Device Correction ...

If it’s not one thing, it’s another. Weeks after the FDA handed down a Class I label to Hamilton Medical’s recall of its ventilators caused by a software conflict, the company has now received a ...

Please provide your email address to receive an email when new articles are posted on . There have been 80 complaints reported to the FDA, but no injuries or deaths. According to the FDA, there are 21 ...

In recent years, as ventilators have become increasingly crucial amid the COVID-19 pandemic, malfunctioning devices have been a constant burr in the FDA’s side. This year alone, the agency has already ...