WAYNE, N.J., May 3, 2017 /PRNewswire/ — Getinge, a leading global provider of products and systems that contribute to quality enhancement and cost efficiency within healthcare and life sciences, today ...
The US Food and Drug Administration (FDA) on Tuesday designated Getinge’s Maquet/Datascope recall of intra-aortic balloon pumps (IABPs) as Class I after five patient deaths were reported since 2016.
The US Food and Drug Administration (FDA) said Tuesday that since notifying physicians of particular intra-aortic balloon pump (IABP) device failures last November, two more patients have died and one ...
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