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Heart Rhythm
Volume 1, Issue 4
, Pages 399-405
, October 2004
Deaths associated with implantable cardioverter defibrillator failure and deactivation reported in the United States Food and Drug Administration Manufacturer and User Facility Device Experience Database
References
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Guidant ICD lead recall # Z-1144/1145-9. Available at http://www.fda.gov/bbs/topics/ENFORCE/ENF00603.html. Accessed February 23, 2004.
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Ventritex ICD pulse generator recall # Z-232/233-7. Available at http://www.fda.gov/bbs/topics/ENFORCE/ENF00472.html. Accessed February 23, 2004.
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This study was funded in part by the Minneapolis Heart Institute Foundation.
PII: S1547-5271(04)00286-3
doi: 10.1016/j.hrthm.2004.05.006
© 2004 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.
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Heart Rhythm
Volume 1, Issue 4
, Pages 399-405
, October 2004
