CHICAGO, July 13, 2020 /PRNewswire/ -- Global medical technology leader Hillrom (NYSE: HRC) today announced the launch of two new respiratory therapy devices: the Volara™ System, which provides ...
(RTTNews) - Baxter International Inc. has issued an urgent medical device recall for certain lots of the Volara system single-patient use circuit and blue ventilator adapter assembly, according to the ...
The US Food and Drug Administration (FDA) published a warning from the medical device company Baxter International Inc, citing problems with their device used for at-home respiratory therapy. The ...
The US Food and Drug Administration (FDA) has changed the warning about the Volara system to a Class I recall, the most severe level of recall, which is reserved for products that may cause injury or ...
Baxter International Inc. (NYSE:BAX) announced today it has issued an Urgent Medical Device Recall for certain lots of the Volara system single-patient use circuit and blue ventilator adapter assembly ...
The Volara system, which joined Baxter’s portfolio following its Hillrom acquisition late last year, connects to a ventilator to provide a trio of respiration treatments to expand the lungs and clear ...
Baxter’s recent recall concerns the Volara lung-expansion therapy device it inherited in its buyout of Hillrom, while Medtronic adds to the long list of issues faced by the now-discontinued HeartWare ...
Baxter is recalling its Volara System Single Patient Use Circuits and Blue Ventilator Adapters because of connectivity issues, the FDA said Sept. 4. The products are circuit components used to connect ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results