Hamilton Medical has recalled ventilators because the devices may fail to restart, the Food and Drug Administration said Thursday. Ventilators that fail to restart may cause low blood oxygen, slow ...

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 ...

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 ...

This hardware recall affected a smaller number of Hamilton’s T1 and C1 ventilators, the latter pictured above, compared to the previous software issue. It also included the MR1, designed for ICUs and ...

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 ...

Sep. 28—Hamilton Medical Center on Monday had 55 COVID patients (47 unvaccinated; 85%); 13 of those were in the intensive care unit (ICU) (12 unvaccinated; 92%); and 10 were on ventilators (10 ...

After the COVID-19 pandemic created an urgent global need for ventilators, a manufacturing line was built in an 86,000-sq-ft Reno warehouse in just one month for an international ventilator company.

RENO – A Reno-based ventilator company has increased production of the critical medical devices by 50 percent in response to the COVID-19 outbreak, expanding production hours to build more than 300 of ...