Court Restricts Philips Respironics CPAP and BiPAP Production
A consent decree of permanent injunction was issued against Philips Respironics, halting production of their sleep therapy devices.
A consent decree of permanent injunction was issued against Philips Respironics, halting production of their sleep therapy devices.
XRP Healthcare and Spiritus Medical announced their strategic collaboration, introducing the Spiritus Vitality Ventilator into East Africa.
Philips Respironics issued an Urgent Medical Device Correction Letter regarding a problem for certain ventilators that could harm patients.
A consent decree of permanent injunction was issued against Philips Respironics, halting production of their sleep therapy devices.
Getinge is recalling several different types of ventilators in its device portfolio that are being labeled as a Class I event by the FDA.
Read MoreBreas Medical USA announced the release and immediate availability of the Xpac by Breas extended life battery for ventilators.
Read MoreNew findings may help guide policy makers in deploying ventilators to states with an urgent need of the technology.
Read MoreNihon Kohden OrangeMed has received U.S. FDA 510(k) clearance for its non-invasive NKV-330 Ventilator System.
Read MoreBackup batteries for GE Healthcare’s CARESCAPE R860 ventilator were recalled because they may run out before they are expected to do so.
Read MoreThe Draeger SafeStar 55 has been identified by the U.S. FDA as a Class I recall, the most serious type of recall.
Read MoreThe Canadian government’s response to ventilator needs of patients early during the pandemic resulted in an excessive equipment surplus.