08192017Headline:

Philadelphia, Pennsylvania

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Jamie Sheller
Jamie Sheller
Attorney • (800) 883-2299

Recall of Another External Defibrillator

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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.