Sleep Apnea Devices Show ‘Very Low’ Amount of Degraded Foam, Philips Says
A recall related to one of Philips sleep apnea devices may not have been as serious or widespread as previously believed.
Read MoreA recall related to one of Philips sleep apnea devices may not have been as serious or widespread as previously believed.
Read MoreJun 30, 2022 | Asset Management | 0 |
If done right, clinical asset management can save money, deter cyberattacks, and help during a crisis. Learn how here.
Read MoreJun 29, 2022 | Batteries, Recalls, Ventilators | 0 |
Backup batteries for GE Healthcare’s CARESCAPE R860 ventilator were recalled because they may run out before they are expected to do so.
Read MoreAmid continued recall concerns, devices from Medtronic and Baxter were recently assigned the most serious recall type be the FDA.
Read MoreJun 23, 2022 | FDA Updates, Ventilators | 0 |
The Draeger SafeStar 55 has been identified by the U.S. FDA as a Class I recall, the most serious type of recall.
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