(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 ...

More than 250 devices have been recalled so far. Baxter Healthcare has issued a Class 1 recall—the most serious type of recall—for Volara systems issued between May 28, 2020 to April 19, 2022. 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 ...

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 ...

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 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 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 ...

Deerfield, Ill. – 2022-06-01 - Baxter International Inc. announced today it has issued an Urgent Medical Device Correction for the Volara System (home care) to reinforce important safety information ...

In back-to-back announcements Thursday, the FDA handed down Class I ratings to recent recalls from Medtronic and Baxter International, identifying that the safety issues carry a high risk of serious ...

A device that’s meant to clear out and expand the lungs may actually go too far, resulting in a potentially dangerous decrease in overall oxygen levels, Baxter said this week. In light of that ...