Recall of Another External Defibrillator

Jamie Sheller
Attorney
(866) 735-1102 Ext 475
Posted by Jamie ShellerJuly 11, 2006 8:11 AM

The FDA has issued a Class 1 recall of Welch Allyn PIC 50 Automated External Defibrillators, manufactured between March 2002 and October 2004. The device may delay or fail to resuscitate the patient. This failure is caused by an eletrical contact problem. During this failure, the device may display various error messages including the "Defib Comm" message.

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