BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Lot Recall for the Medi-Trace™ Cadence Adult and Pediatric Radiotransparent Defibrillation Electrodes, Covidien

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 02203/13

Covidien has issued a Field Safety Notice concerning a recall of several lots of the Medi-Trace™ Cadence Adult 22550R and Pediatric 22550P Radiotransparent Defibrillation Electrodes. On the lead wire arcing/sparking, or thermal damage may occur, which could result in impairment of the defibrillation therapy.

Lot Recall for the Medi-Trace™ Cadence Adult and Pediatric Radiotransparent Defibrillation Electrodes, Covidien , Download_VeroeffentlichtAm_EN PDF, 20KB, File does not meet accessibility standards