Guidant Corporation - Zoom Latitude Programming System - Class 3
Guidant Zoom Latitude Programming System, model 3120, A portable cardiac rhythm management system designed to be used with Guidant implantable pulse generators. Guidant Corporation, 4100 Hamline Avenue North, St. Paul, MN 55112-5798
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Guidant Corporation - INSIGNIA Entra and NEXUS Entra - Class 2 Recall
Guidant INSIGNIA I Entra-- family of pacemakers includes the following: --The INSIGNIA I Entra pacemakers are multiprogrammable pacemakers from Guidant. Guidant Corporation, Cardiac Rhythm Management, 4100 Hamline Avenue North
Guidant Corporation - VENTAK PRIZM 2 - Class 2 Recall
Guidant VENTAK PRIZM VR (model 1860) and VENTAK PRIZM DR (model 1861) Automatic Implantable Cardioverter Defibrillator (AICD), Guidant Corporation, Cardiac Rhythm Management, 4100 Hamline Avenue North, St. Paul, MN 55112-5798 USA.
Guidant Corporation - VITALITY and VITALITY 2 - Class 2 Recall
VITALITY (models 1870, 1871, T125, T127, T135) and VITALITY 2 (models T165, T167, T175, T177). Implantable Cardioverter Defibrillators (ICD). Quantities Distributed by model are as follows: VITALITY model 1870 = 40, model 1871 = 1,
FDA Issues Nationwide Notification of Recall of Certain Guidant
FDA is notifying health care providers and patients that the Guidant Corporation is recalling certain of its implantable defibrillators and cardiac resynchronization therapy defibrillators. These devices can develop an internal short
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Guidant Defibrillator Targeted in Wrongful Death Lawsuit
After three years of not telling patients and physicians about the defect in the Prizm 1861, Guidant finally issued a recall on June 17, 2005. While they reported then that approximately 13900 Prizm 1861 devices manufactured before the
Guidant/Medtronic Litigtaion Continues
The litigation continues as Guidant Corporation has issued yet another recall of their popular defibrillator and pacemaker devices. This most recent recall affects over 27000 devices and is in connection to an internal mechanism defect

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Guidant Recall - Guidant Pacemaker Defibrillator Recall
Learn about the Guidant Recall. Guidant, a large manufacturer and distributor of implantable cardioverter defibrillators (ICD) and devices for cardiac
Patient Communications Providing Important Safety Information
If you have questions about the materials on this page, call Guidant for more information. Patients and Families: 1-866-GUIDANT (1-866-484-3268)
Guidant Lawsuit | Guidant Recall of Heart Defibrillators, Pacemakers
For free answers to your questions about the Guidant recall, please call us toll-free at 1-800-883-8888 or complete this online contact form.
Guidant Defibrillator Recall Lawyer Lawsuit for Guidant
Guidant Defibrillator Recall Lawyer Lawsuit for Guidant defibrillator malfunction.
Guidant Lawsuit, Guidant Pacemaker Recall, Heart Device Recall
Guidant lawsuit, if you or a loved one has a heart device, consult your physician immediately to confirm that your device has not been recalled.
Guidant Class Action Lawyers: Guidant Defibrillator Resources
Guidant Defibrillator Resources. Learn more about the Guidant Recall and Guidant Heart Devices. More extensive Guidant device historical reliability data is
GUIDANT PACEMAKER* RECALL (implantable cardioverter-defibrillators)
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Guidant Recall Lawsuit and Lawyers - Comprehensive Information
Our firm, Lieff Cabraser Heimann & Bernstein, LLP, is representing Guidant patients across the US in personal injury lawsuits seeking damages for the guidant+recall: california defibrillator guidant recall | attorney california defibrillator guidant recall | california defibrillator guidant recall | attorney california defibrillator guidant recall | guidant+recall