Guidant recalls Contak Renewal and Contak Renewal 2
2006.01.20
Product group Active implantable medical devices
Reference 02284/04
Guidant Corp. recalls Contak Renewal, model 135 and Contak Renewal 2, model 155 due to possible deterioration in a wire insulator within the lead connector block resulting in an electrical short while delivering shock therapy and loss of device function.
Update of the recall dated June 23, 2005
Guidant recalls Contak Renewal and Contak Renewal 2 , Download_VeroeffentlichtAm_EN