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Guidant Recalls 50,000 Defibrillators
By ASHLEY M. HEHER, Associated Press Writer
INDIANAPOLIS - Guidant Corp. said Friday it was recalling cardiac defibrillators implanted in nearly 50,000 people worldwide because of a flaw that could cause it to malfunction.
At least two patients with the devices have died. The Indianapolis-based company said it was advising physicians about the safety of several defibrillator models, which have failed at least 45 times.
The U.S.
Food and Drug Administration advised patients to see their doctor and said it would not recommend whether individual patients with one of the recalled devices should have them removed and replaced. Guidant offered to replace some of the defibrillators, but has not said that removal or replacement of any is necessary.
Read more here
By ASHLEY M. HEHER, Associated Press Writer
INDIANAPOLIS - Guidant Corp. said Friday it was recalling cardiac defibrillators implanted in nearly 50,000 people worldwide because of a flaw that could cause it to malfunction.
At least two patients with the devices have died. The Indianapolis-based company said it was advising physicians about the safety of several defibrillator models, which have failed at least 45 times.
The U.S.
Food and Drug Administration advised patients to see their doctor and said it would not recommend whether individual patients with one of the recalled devices should have them removed and replaced. Guidant offered to replace some of the defibrillators, but has not said that removal or replacement of any is necessary.
Read more here