Baxter International Inc.

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FDA Says Baxter Healthcare Recalls Volara System For Risk Of Respiratory Distress In Some Patients

Published: 06/23/2022 15:05 GMT
Baxter International Inc. (BAX) - :fda Says Baxter Healthcare Corporation Recalls Volara System for Risk of Respiratory Distress in Ventilated Patients During Home Use.
FDA Says Has Identified Recall of Volara System As a Class I Recall.
FDA Says There Has Been One Complaint and One Injury, As Well As Two Deaths, Associated With the Use of Volara System Device.
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