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Spokane, Washington  Est. May 19, 1883

Guidant Corp. issues pacemaker warning

Associated Press

INDIANAPOLIS — Guidant Corp. on Monday warned physicians that replacements might be needed for nine pacemaker models made between 1997 and 2000, of which some 28,000 remain implanted in patients worldwide.

The Indianapolis-based company, which last month recalled almost 109,000 defibrillators, released a warning that says a sealing component in the pacemakers has degraded in some cases, resulting in higher-than-normal moisture in the devices and possible malfunction.

About 78,000 of the pacemakers were distributed, with about 18,000 remaining in U.S. patients, the company said in the statement. The devices, which send electrical pulses to the heart to accelerate a slow heart beat, have a seven- to 10-year life span before they must be replaced.

Guidant said it has identified 69 failures among the pacemakers — all after they had been used for at least 44 months. The models include: Pulsar Max, Pulsar, Discovery, Meridian, Pulsar Max II, Discovery II, Virtus Plus II, Intelis II, and Contak TR.

The company told physicians they should consider replacing the devices for patients who are dependent on the devices. Pacemakers are about the size of two half dollars held together.

Several patients implanted with the devices have lost consciousness or developed possible heart failure, Guidant said. It reported the death of one person whose pacemaker may have failed, but said the role of the device could not be confirmed as it was not returned for testing.

Food and Drug Administration spokeswoman Julie Zawisza said the agency was evaluating Guidant’s warning. The company said the FDA may classify the warning as a recall. Guidant issued two safety warnings last month for 11 models of defibrillators that were later classified by the FDA as recalls.

Defibrillators, three times the size of pacemakers, are also implanted; they shock the heart back into rhythm when it beats too quickly. Almost 88,000 of the Guidant devices that were recalled remain implanted worldwide.

The problem with Guidant’s pacemakers poses less of a risk for patients than that of its defibrillators, according to Dr. Angel Leon, chief of cardiology at Emory Crawford Long Hospital in Atlanta. That’s because of the relatively small number of pacemakers implanted and because the degradation that can occur does so gradually, allowing patients more time to seek help.