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Medtronic Recalls Cobalt XT, Cobalt and Crome ICDs and CRT-Ds for Risk that Devices May Issue a Short Circuit Alert and Deliver Reduced Energy Shock During High Voltage Therapy

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.

Crome icdsContact medtronic technical servicesDrug administrationMedtronic technical servicesCrome implantable cardioverter defibrillatorsResynchronization therapy defibrillatorsCardiac resynchronization therapy defibrillatorsExternal link disclaimerActive canLead impedance alert

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