Correction of LIFEPAK® 12 und LIFEPAK® 20, Medtronic
2006.05.03
Product group Medical electronics / Electromedical devices
Reference 00900/06
Medtronic Emergency Response Systems is conducting a correction of their LIFEPAK® 12 und LIFEPAK® 20 defibrillator and monitors manufactured between October 2005 and February 2006. These devices contain a therapy connector that may have one or more connector sockets that do not meet the design specifications.
Correction of LIFEPAK® 12 und LIFEPAK® 20, Medtronic , Download_VeroeffentlichtAm_EN