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Guidant Pacemaker | Defibrillator Recall News Article |
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| July
28, 2005 |
Star
Tribune (Indianapolis), "Guidant
promises openness" |
While
defending its actions over a recent spate of
recalls of its heart devices, a Guidant Corp.
executive acknowledged that the industry is
entering a new era of disclosure, with doctors
demanding more information on product safety
than ever before.
The medical technology
company, which makes heart defibrillators and pacemakers at its campus in Arden
Hills, has come under fire in recent weeks for failing to notify doctors early
on that some of its implantable cardiac defibrillators could malfunction on rare
occasions.
"People wish to know
more, so we will provide more quality performance information in greater quantity
and with greater frequency. Plain and simple," said Fred McCoy, president
of Guidant's $2.5 billion cardiac rhythm management division, in an interview
with the Star Tribune earlier this week.
Any change in the
way product reliability information is distributed would not only affect the
thousands of increasingly inquisitive patients who will receive the life-saving
devices in coming years, but the local companies that make them, including Medtronic
Inc. and St. Jude Medical Inc. |
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| Founded in 1972, Lieff Cabraser
Heimann & Bernstein, LLP is an over-sixty-attorney
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Our lawyers
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