LUCAS 2 Chest Compression System. Designed to uninterrupted chest
compressions at a consistent rate and depth. Recall # Z-1664-2011
RECALLING FIRM/MANUFACTURER
Jolife AB, Lund, Sweden, by letter dated February 2011. Firm initiated
recall is ongoing.
REASON
LUCAS 2 Chest Compression System may have malfunctions resulting from
the failure of a hood probe on the device that connects to the
battery.
The device may stop in fail safe mode and the LEDs will start
flickering
or the device will switch off.
VOLUME OF PRODUCT IN COMMERCE
1,843 units
DISTRIBUTION
Nationwide and Internationally

For more information, including serial numbers of recalled devices, go
to http://www.fda.gov/Safety/Recalls/EnforcementReports/ucm248171.htm.

Tim Erskine
3/24/2011 6:44 PM

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