The Food and Drug Administration has approved Maquet’s FLOW-i anesthesia system for 510(k) marketing, according to a MedGadget report. The anesthesia machine features advanced monitoring and ...

Draeger Medical, or Dräger US, recalled more than half a million airway devices because of a manufacturing error that can lead to hypoxia and death, the FDA said May ...

The FDA recalled SpaceLabs Healthcare’s Arkon anesthesia delivery system for going into a “failed state.” 1. The Class 1 recall covers 253 units manufactured between Sept. 21, 2012, and Sept. 28, 2017 ...

The FDA issued a recall for Spacelabs Medical’s Spacelabs Anesthesia Workstations and Service Kits that provide oxygen, air and nitrous oxide through patient breathing circuits. Some CAS Absorbers are ...

In today’s anesthesia machine market, the high-acuity/top-tier systems have become the fastest growing segment. This spot was once held by the mid-acuity systems, which were often the “go-to” machines ...

As ventilators and other respiratory devices became more crucial than ever throughout the COVID-19 pandemic, so too did any safety issues embedded in the machines become more apparent. Following in ...

JACKSON, Mich.--(BUSINESS WIRE)--Plexus Technology Group, LLC (Plexus TG), a market-leading, best-of-breed provider of anesthesia information management systems (AIMS), announces that its AIMS, ...

This growth is driven by the increasing prevalence of respiratory diseases, rising number of surgical and critical care ...