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 ...

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 ...

Hamilton Medical’s ventilator recall was recently given a Class I designation from FDA. The company originally contacted customers in June after learning that its C1, C2, C3, and T1 ventilators with ...

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 ...

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 ...

Hamilton Medical notified customers of a malfunction with its HAMILTON-TI ventilators with software versions 1.1.2 and lower in which the correct amount of oxygen may be miscalculated, according to ...