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Guidant Defibrillator and Pacemaker Recall Warning Letters

Did You Know?
Common signs of pacemaker failure include shortness of breath, dizziness, lightheadedness or a prolonged fast heart rate.

Guidant has issued the following doctor warning letters and patient warning letters relating to its defibrillators and pacemakers as indicated below. Click on the links by each listed letter to read a copy in PDF format.

Note: Guidant Warning Letters will be posted on this page as they are released.

Release Date: July 22, 2005
Physician Letter Revised Recommendations (Update) re Ventak Prizm AVT, Vitality AVT and Contak Renewal AVT

Release Date: July 18, 2005
Physician Letter re Pulsar Max, Pulsar, Discovery, Meridian, Pulsar Max II, Discovery II, Virtus Plus II, Intelis II and Contak TR

Release Date: June 24, 2005
Patient Letter re Contak Vitality AVT and Contak Renewal AVT

Release Date: July 15, 2005
Patient Letter re Contak Renewal 3 and 4

Release Date: June 24, 2005
Patient Letter re Ventak Prizm 2 DR

Release Date: June 24, 2005
Patient Letter re Ventak Prizm AV

Release Date: June 23, 2005
Physician Letter re Contak Renewal 3 and 4, Contak Renewal 3 and 4 AVT, and Renewal RF

Release Date: June 17, 2005
Physician Letter re Ventak Prizm 2 DR

Release Date: June 17, 2005
Physician Letter re Contak Renewal & Contak Renewal 2

If you are in need of legal advice about your Guidant Defibrillator or Guidant Pacemaker, or simply wish to speak to an attorney who has experience with Guidant Recall in your state, you may use our Free Online Consultation Form.

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What Guidant product was installed?
Guidant Defibrillator
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