| Subject: | FDA Announces Class 1 Recall of ZOLL AED Plus Defibrillator |
| Category: | Food and Drug Administration (FDA)
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| Published: | Thu, 9 Apr 2009 - 02:00 pm |
| The Food and Drug Administration (FDA) and ZOLL Medical Corporation have notified healthcare professionals of a Class 1 Recall of ZOLL AED Plus Defibrillators distributed from May 2004 through February 9, 2009. The Recall was initiated because the device may fail to deliver a defibrillation shock, which could result in failure to resuscitate a patient during treatment of sudden cardiac arrest. On February 12, 2009 and March 31, 2009, the company sent their distributors and customers recall... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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