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 Icds Contact Medtronic Technical Services Drug Administration Medtronic Technical Services Crome Implantable Cardioverter Defibrillators Resynchronization Therapy Defibrillators
Source: dicardiology.com