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FDA OKs Nihon Kohden’s Ventilator System

Nihon Kohden OrangeMed has received U.S. FDA 510(k) clearance for its non-invasive NKV-330 Ventilator System.

Getinge is recalling the Flow-c and Flow-e anesthesia systems after reports of cracked or broken on/off switches on the system’s suction unit.

Jun 30, 2022 | Recalls | 0 |

A recall related to one of Philips sleep apnea devices may not have been as serious or widespread as previously believed.

Jun 30, 2022 | Asset Management | 0 |

If done right, clinical asset management can save money, deter cyberattacks, and help during a crisis. Learn how here.

Backup batteries for GE Healthcare’s CARESCAPE R860 ventilator were recalled because they may run out before they are expected to do so.