Recall Date: 10/30/2008 |
Title: 2008 CR Plus recall: |
Units: LIFEPAK CR Plus |
Issue: This recall is being conducted due to the device being configured with the incorrect software for semi-automatic instead of fully automatic use. When the device is needed for a cardiac arrest emergency, the device will require that the user press the shock button instead of automatically delivering a shock as per the normal operation of the fully automatic device. |