Another Welch Allyn Defibrillator Recall

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Another Welch Allyn Defibrillator Recall

November 8th, 2007 amy

Welch Allyn has announced another Class I defibrillator recall, this time for 1,794 AED10 Automatic External Defibrillators. These defibrillators, used by medical professionals to shock the heart of a cardiac arrest patient back into rhythm, may malfunction and fail to resuscitate the patent.

Per the company’s press release, they have observed 49 failures in the manufacture of the AED10 defibrillators and have received 3 customer complaints which the company deems an unacceptable risk. The potentially defective defibrillators were manufactured between March 29, 2007 and August 9, 2007 at the Welch Allyn Protocol, Inc. facility in Beaverton, OR.

This is the second Welch Allyn defibrillator recall in three months, the third in a year and a half. The MRL/Welch Allyn AED 20 Automatic External Defibrillators were recalled twice, most recently in August 2007 and previously in June 2006.

Customers should have already received recall notices from the company. Owners of these defibrillators may contact Welch Allyn at 1-800-462-0777 option 4 to arrange for an exchange unit.

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