
After two generations of battery-prodded hearts, thousands are left with faulty wiring.
This summer, the U.S. Food and Drug Administration (FDA) issued a public recall based on that reality. The targets were certain Medtronic Kappa and Sigma pacemakers.
About 21,000 patients were affected.
The FDA warned those with the recalled implants of symptoms ranging from abnormal heart rate to lightheadedness.
Joseph DeToia, 86, of White Plains, though personally unaffected by the Medtronic recall, has had his fair share of concerns with a similar device.
“I delivered pharmaceuticals to nursing homes and one day, I couldn’t walk up the steps,” said the former U.S. Navy man. “I had to go in and the nurse asked me what was wrong. She said, ‘You had better see a doctor right away.’”
DeTaio went to Cardiology Consultants of Westchester and had a defibrillator installed 10 years ago.
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