MedPage Today -- WASHINGTON -- The FDA issued a class I recall -- its most serious -- of several St. Jude Medical 6 French Engage Introducer devices because its shaft or hub assembly may break and cause potentially fatal bleeding.
MedPage Today -- WASHINGTON -- The FDA issued a class I recall -- its most serious -- of several St. Jude Medical 6 French Engage Introducer devices because its shaft or hub assembly may break and cause potentially fatal bleeding.
