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FDA Warns Users About Faulty Components in 14 External Defibrillator Models
Date:4/27/2010

milar software updates for other affected devices. However, FDA's review of the updated software indicates that the software detects some, but not all, identified defects.

Nihon Kohden is based in Tokyo, Japan. GE Healthcare is located in Britain.

For more information

Defective Cardiac Science Corporation Powerheart, CardioVive, Nihon Kohden, and GE Responder External Defibrillators:  Updated April 27, 2010

http://www.fda.gov/MedicalDevices/Safety/AlertsandNotices/ucm191426.htm

Media Inquiries: Karen Riley, 301-796-4674, karen.riley@fda.hhs.gov

Consumer Inquiries: 888-INFO-FDA


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SOURCE U.S. Food and Drug Administration
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