Software Bug Leads to Recall of Puritan Bennett Ventilators
The FDA announced on November 7 that it has notified healthcare facilities of the Class 1 recall of certain Nellcor Puritan Bennett 980 ventilator systems.
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CareFusion Ventilators Recalled
On October 10, the FDA announced a Class 1 recall of CareFusion’s EnVE and ReVEL ventilators, related to possible power connection failure.
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Critical Care Ventilator
At the European Society of Intensive Care Medicine annual congress in Barcelona, GE Healthcare introduced the Carescape R860, a critical care ventilator designed to overcome the dangers of Ventilator-Induced Lung Injury.
Read MoreVentilator Summit: Improvements Needed in Terminology, Training
At last week’s annual AAMI/FDA summit on ventilator technology, an emphasis was placed on the importance of standardizing the terms used to describe the technology as well as the urgent need for better training.
Read MoreAAMI Podcast Series to Debut
AAMI is partnering with Healthcare Tech Talk hosts Terry Baker and Kelley Hill to launch an AAMI podcast series featuring interviews with leaders and experts in healthcare technology. The episodes will be available for download on the AAMI podcast page and through iTunes, TuneIn, and Stitcher.
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