Philips Respironics BiPAP and CPAP Masks Hit by Recall
Philips has recalled certain masks used with bilevel positive airway pressure machines and CPAP machines due to a serious safety concern.
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Malfunctioning Integra Intracranial Monitor Was Used on Patient Who Died: FDA
The U.S. FDA has identified one patient death that was tied to the use of Integra LifeSciences CereLink ICP monitors.
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Hamilton Medical Recalls Intensive Care Ventilator Due to Potential Breathing Support Defect
Hamilton Medical AG is recalling an intensive care ventilator after complaints revealed a hardware issue with its status indicator board.
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Certain Philips Respironics BiPAP Machines Recalled Due to a Plastic Issue, FDA Says
Philips recalled certain bi-level positive airway pressure machines that may contain a plastic contaminated with a non-compatible material.
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A New Type of Defibrillator Met Safety, Effectiveness Goals in Clinical Study
A new extravascular implantable cardioverter-defibrillator met safety and effectiveness goals for participants in a premarket clinical study.
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