This recall addresses potential component defects that may affect approximately 280, between August 000 AEDs manufactured, august 2003 and, 2009. As previously announced by the Company, the corrective action includes a software update designed to enable the AED’s self-test to detect failed elements. The program update is already available for some AED versions and thousands of users have previously downloaded and installed the revise. NEW UNITS AREN’T AFFECTED. THE BUSINESS improved its manufacturing processes in August, 2009. All units produced by the Company since, including units for sale and shipped currently, are not suffering from this presssing issue. THE RECALL HASN’T EXPANDED. The FDA clarified the list of affected AEDs to include those the business manufactures for Nihon Kohden and General Electric .Bonding together with your kids in the current tech-obsessed world Next time you end up at a busy cafe, have a look around at the youngsters. Young tikes all of the real way to old teens are bound to possess some type of techno-gadget within their hands. Just last year, AVG Digital Diaries shared their findings on what the web is impacting children today. They discovered that 42 % of parents had been worried that their kids were spending a lot of time on products. Also, 43 % had been concerned that their kids didn’t get outside enough.