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Guidant recalls Ventak AV heart defibrillators for adjustment
Guidant Corp recalls about 2 000 Ventak AV implantable defibrillators after a programming error can cause the heart to race. Doctors will modify devices non surgically using a radio transmitter. The issue has not caused deaths and the FDA approved Guidant’s fix method while stock moved on the news.
MENTIONED IN THIS ARTICLE
Indianapolis
Ventak AV
Guidant Corp
United States
U.S
Douglas Zipes
Indiana University Medical School
Zipes
Hugh Calkins
Johns Hopkins Hospital
Baltimore
Food and Drug Administration
Guidant
FDA
Sharon Snider
Ventak
Carol Lindahl
Eli Lilly & Co
New York Stock Exchange