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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 500 Results *
Recall Date to: 05/24/2015
 
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Z-800 Volumetric Infusion System. For intravenous infusion of parenteral fluids, blood and blood ... 2 03/29/2013 Zyno Medical LLC
IF 8000; 1/F Interferential Electrical Stimulation Device; NMES (neuromuscular electrical stimulatio... 2 06/26/2014 Zynex Medical, Inc.
Mouse anti-TTF-1 concentrate used in a panel designed to differentiate between different types of ca... 2 10/09/2004 Zymed Laboratories Inc.
Mouse anti-TTF-1 2nd Gen Predilute used in a panel designed to differentiate between different types... 2 10/09/2004 Zymed Laboratories Inc.
ZOLL E Series Defibrillator/Pacemaker/Monitors, BLS Model, with software versions 4.XX, 6.XX and 7.0... 2 05/07/2010 ZOLL Medical Corporation, World Wide Headquarters
ZOLL R Series Defibrillator/Pacemaker/Monitor Used by qualified medical personnel for the purpose... 2 09/29/2009 ZOLL Medical Corporation, World Wide Headquarters
Zoll AED Plus Defibrillator 1 04/01/2009 ZOLL Medical Corporation, World Wide Headquarters
Zoll E Series Defibrillator with 12 Lead ECG, Automated external defibrillator, Software Version 3.0... 2 06/28/2008 ZOLL Medical Corporation, World Wide Headquarters
Zoll Medical X Series, PropaqMD, PropaqM Defibrillator/Pacemaker/Monitor With System Software Ver... 2 03/31/2014 ZOLL Medical Corporation
Zoll X Series Defibrillator/Pacemaker/Monitor Product Usage: The product is used by qualified me... 2 09/17/2012 ZOLL Medical Corporation

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