LIFEPAK 20/20e defibrillator/monitor.
Specific serial numbers are affected.
This is an acute cardiac care device used in clinical and hospital settings. It has a dual power supply system and is designed to operate on AC (mains) power or DC (battery) power.
Devices with specific serial numbers, manufactured from 31 July 2002 to 9 February 2009 inclusive, are affected. See the manufacturer’s
Field Safety Notice
for a list of the relevant serial numbers.