FDAMay 24, 2018device

Perseus A500 Anesthesia Machine; Cat. no. MK06000 Product V Product Usage: Intended for use in anesthetizing adults, children, and neonates and can be used for automatic and manual ventilation, pressuresupported spontaneous breathing, and spontaneous breathing. Perseus is equipped with airway mon...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The Draeger anesthesia device may be able to dose 100% N2O. In the event of a fault, the S-ORC module would not prevent setting an N2O flow that would result in a hypoxic mixture from being dosed to the patient. Potential adverse outcomes include death of the patient.

What to do

FDA enforcement status: Terminated

Brands named

draeger medicaldraeger

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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