We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » Eitan Medical Recalls Infusion Pumps for Failure to Detect Air in the Line
Eitan Medical Recalls Infusion Pumps for Failure to Detect Air in the Line
Eitan Medical’s recall of 1,323 infusion pumps — for a risk that the pump may fail to detect air in the line when running on battery power — has been identified by the FDA as Class I, the most serious type of recall as use of these devices may cause serious injuries or death.