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Ra Medical Systems Gets FDA 510(k) Clearance for DABRA 2.0 Catheter

Ra Medical Systems received U.S. FDA 510(k) clearance for its DABRA 2.0 catheter as part of the DABRA Excimer Laser 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.