FDA: Urgent Correction for Baxter Volara System
Baxter issued an Urgent Medical Device Correction notice for all Volara System patient circuits to be corrected prior to continued use, according to an FDA alert.
Tag: Volara System
FDA: Urgent Correction for Baxter Volara System
Baxter issued an Urgent Medical Device Correction notice for all Volara System patient circuits to be corrected prior to continued use, according to an FDA alert.
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Products 2025: Secretion Clearance & Suction
A closer look at suction and secretion clearance devices from ABM Respiratory, Baxter, Neotech, Philips, Precision Medical, Sentec, Seoil Pacific, and Tactile Medical.
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Baxter Recalls Certain Volara Circuits and Blue Ventilator Adapter Assemblies
Baxter Healthcare Corp recalls certain Volara system single-patient use circuits and blue ventilator adapter assemblies due to disconnection risk that may prevent proper ventilation.
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Baxter Recalls Volara System Parts Due to Ventilator Disconnection Risk
The recall affects specific lots of the Volara system single-patient use circuit and blue ventilator adapter assembly due to a potential disconnection issue that could disrupt ventilation.
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Class I Recall for Hillrom Volara System
Baxter International Inc has issued an Urgent Medical Device Correction for the Hillrom Volara System (home care) over a possible risk of oxygen desaturation or barotrauma.
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