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Pacemakers recalled over risk of electrical short

The Food and Drug Administration (FDA) has issued a recall of nearly 62,000 heart-health” target=”_blank”>pacemakers< “If the device is unable to deliver pacing, patients may experience slow or irregular heartbeat, fainting, shortness of breath, tiredness, dizziness or discomfort,” the FDA said, on its recall notice. “Additionally, shorter battery life and …

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