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U.S. Department of Health and Human Services

Medical Device Recalls

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11 to 20 of 500 Results *
Recall Date to: 10/20/2014
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Product Description
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FDA Recall
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Recalling Firm
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Zoll E Series BLS Defibrillator/Pacemaker/Monitor Software versions 7.10 and 7.11 The product is... 2 05/25/2011 ZOLL Medical Corporation
Zoll M Series Automated Defibrillator (AED) 2 09/17/2004 Zoll Medical Corporation
Zoll M Series External Defibrillator 2 07/10/2003 Zoll Medical Corporation
Zoll AED Plus Defibrillator (Automatic External Defibrillator) 2 02/06/2003 Zoll Medical Corporation
Model 4000 Monitor component of the LifeVest Wearable Defibrillator 2 12/16/2010 Zoll Lifecor Corporation
Monitor portion of the LifeVest device - specifically the Defibrillator printed circuit assembly (PC... 2 01/28/2009 Zoll Lifecor Corporation
Battery Pack portion of the LifeVest device. The LifeVest is a wearable cardioverter defibrillator w... 3 10/18/2007 Zoll Lifecor Corporation
Electrode Belt, component of the LifeVest Wearable Defibrillator, Product number 10A0889-A01. Specif... 2 06/15/2007 Zoll Lifecor Corporation
Zoll Circulation LifeBand Single Pack (accessory), and Nickel-metal hydride (NIMH) Battery. The Li... 3 07/22/2014 Zoll Circulation, Inc.
AutoPulse Resuscitation System Model 100, Mfg by:Zoll Circulation Sunnyvale, CA. The AutoPuls... 2 01/09/2013 Zoll Circulation, Inc.

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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