Recall of LIFEPAK EXPRESS AED, LIFEPAK CR Plus AED LIFEPAK 1000 defibrillator, or LIFEPAK 500 Biphasic AED

According to Republic of Lebanon Ministry of Public Health, this recall involved a device in Lebanon that was produced by Physio-Control Australia.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here


  • Manufacturer Parent Company (2017)
  • Source