The Food and Drugs Administration (FDA), United States posted a medical device safety alert concerning AutoPulse Resuscitation System Model 100, manufactured by Zoll Circulation, Inc.

According to the report, there were complaints associated with an unexpected stop in AutoPulse compressions.

For details, please visit the following FDA website:
http://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-0658-2013&w=01162013&lang=eng

If you are in possession of the product, please contact your supplier for necessary actions.

Posted on 21 January 2013