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U.S. Department of Health and Human Services

Safety

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Welch Allyn PIC 50 Automated External Defibrillators

Audience: Emergency services personnel and risk managers

[Posted 07/07/2006] MRL, Inc., and FDA notified healthcare professionals of a Class I recall of Welch Allyn PIC 50 Automated External Defibrillators, catalog #97108X manufactured from March 2002 through October 2004. An electrical contact problem may result in the device's failure to provide a defibrillation shock, that could result in delay or failure to resuscitate the patient. This failure may be accompanied by various error messages on the display panel, including the "Defib Comm" error message.

[June 30, 2006 – Recall Notice – FDA]

Related MedWatch Alerts:

[June 12, 2006] Welch Allyn AED20 Automatic External Defibrillators