(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 ...
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 ...
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 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 ...
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, on the heels of its Life2000 ventilator recall, yesterday announced the recall of certain lots of the Volara system single-patient use circuit and blue ventilator adapter ...
A respiratory device that Baxter inherited through its $12.5 billion Hillrom acquisition might work a little too well, a problem that prompted the company to issue an urgent medical device correction.
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 ...
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 ...
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