An “Urgent Medical Device Correction” issued by Abbott-Thoratec for its HeartMate II LVAS Pocket System Controller has been classified by the US Food and Drug Administration (FDA) as a class I recall, ...
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May 4, 2009 (Paris, France) — A product information page on the website of left-ventricular-assist device (LVAD) manufacturer Thoratec (Pleasanton, CA) boasts that "with product attributes ...
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