Corrective action affecting the ICD-models VITALITY HE, RENEWAL 3 and 4 manufactured by Guidant Corp.
2006.05.26
Product group Active implantable medical devices
Reference 01393/06
Guidant Corp. informs about a corrective action due to possible therapy failure affecting ICD-models VITALITY HE, RENEWAL 3 and 4, if the device is implanted sub-pectoral with the serial number facing down.
Advisory Notice is only available in German language.