The devices, which are made by Philips Medical Systems ... distributed between 2005 and 2012 under the names HeartStart FRx, HeartStart HS1 Home, and HeartStart HS1 OnSite. The recall of these ...

The FDA says an electrical problem with recalled Philips' HeartStart devices could cause ... In Canada, Philips recalled the FRX and HS1 AED device in March and sent information letters to ...