The FDA has issued a Class I recall for multiple anesthesia breathing circuit kits due to cracks in the hose that could cause inadequate ventilation. The affected products include VentStar 220 as well ...
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 ...
Kit Check, a provider of hospital pharmacy kit automation, announced the launch of Anesthesia Check, a cloud-based software tool to manage and track medications in the operating room. Anesthesia Check ...
> The FDA has placed its most serious warning on Cardinal Health's ($CAH) recall of anesthesia kits designed for presurgery. More > The lack of child-sized medical ...
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