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Information for subsets of INSIGNIA and NEXUS pacemakers from Guidant

Product group Active implantable medical devices
Reference 01794/06

GUIDANT informs about potential for malfunction and device withdrawal in a subset of INSIGNIA and NEXUS pacemakers, CONTAK RENEWAL TR/TR2 CRT-pacemakers, and VENTAK PRIZM 2, VITALITY and VITALITY 2 ICDs.

Update of the notification issued on July 4, 2006.

Advisory Notice is only available in German language.

Information for subsets of INSIGNIA and NEXUS pacemakers from Guidant , Download_VeroeffentlichtAm_EN PDF, 169KB, File does not meet accessibility standards