FDAFebruary 8, 2017device

Arkon Anesthesia Delivery System, Model 99999. Product Usage: Continuous Ventilator The Arkon Anesthesia Delivery System is designed to provide emergency oxygen, vaporized agent delivery and manual ventilation in the event of a power failure scenario. Clinicians are able to use Emergency O2 and m...

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

The hazard

Spacelabs has received reports of the Arkon Anesthesia Delivery System, Model 99999, shutting down without warning. The power supply has failed in a way that does not trigger the normal on battery alarms.

What to do

FDA enforcement status: Terminated

Brands named

del mar reynolds medicaldeldel mar

Recall history

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

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