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: Philadelphia Personal Injury LawyerRecall of External Defibrillators
By Jamie Sheller
Welch Allyn Protocol voluntarily recalled more than 14,000 automatic external defibrillators. This action is a Class 1 recall, the most serious type, which is used when it is reasonably probable that the produce can cause serious bodily injury or death. The recalled products are AED 10 and MRL JumpStart external defibrillators manufactured between October 3, 2002 and January 25, 2007. According to Welch Allyn Protocol, the recalled defibrillators have a risk of shock, blown fuses and device shutdown, that can lead to death. Customers can exchange their device for a similar one or receive a discount on a new defibrillator.
Originally posted at InjuryBoard by Jamie Sheller
Full post as published by Philadelphia Personal Injury Lawyer on March 29, 2009 (boomark / email).
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