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FDA Updates Consumers on Guidant Corporation’s Implantable Defibrillators

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Guidant Recall Lawyers - Guidant Defibrillator Recall

 
Guidant Recall Lawyers
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(800) 486-4450 

 

Vernon J. Petri
Attorney At Law

 2124 East Hanna Ave.
Indianapolis, Indiana
46227-3314
(317) 780-6610
Fax: (317) 780-6620
VJPetri@Petrilaw.com

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Malfunctions in these devices can lead to serious consequences and it’s important for patients to call their doctor for additional information and personalized advice,” said Daniel Schultz, MD, Director of FDA’s Center for Devices and Radiological Health.

As the Food and Drug Administration (FDA) continues to evaluate the safety and performance of certain implantable defibrillators manufactured by Guidant Corporation, the Agency has now classified the recalled devices. This additional information on the relative health risks of the devices will help patients and doctors take appropriate action, if necessary.  ...more

Guidant Postings

Guidant has posted information for patients and physicians on its web site at http://guidant.com/physician_communications/. If you have further questions, you may contact Guidant at 1-866-GUIDANT (1-866-484-3268).

FDA - MedWatch

If you are a physician or a patient who has experienced a problem with any of the affected defibrillator models, please send a report to FDA's MedWatch program and to Guidant. See: http://www.fda.gov/medwatch/index.html for filing information or call 1-800-FDA-1088 (1-800-332-1088).