FDA issues Class I recall on St. Jude?s defibrillator leads

[ahlam1399]

FDA issues Class I recall on St. Jude?s defibrillator leads

FDA issues Class I recall on St. Jude?s defibrillator leads
Jan 22 (Reuters) - St. Jude Medical Inc said the U.S. Food and Drug Administration has issued a Class I recall on faulty parts of its devices implanted into patients to control irregular heartbeats.

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