FDA issues recall on J&J heart device
(Reuters) - The U.S. Food and Drug Administration on Tuesday issued a recall of a heart device made by a unit of Johnson & Johnson due to a faulty valve, following a recall by the company in June.
from Reuters: Health News http://reut.rs/2qjdKwj
http://bit.ly/2zwRqiM
January 03, 2018
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