The Food and Drug Administration has classified the recall of a deep brain stimulation device (DBS) as Class I, meaning that the agency believes there is “a reasonable probability” that the use of the product “will cause serious adverse health consequences or death.” http://www.fda.gov/Safety/Recalls/ucm350691.htm In an interesting twist, in response..
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Date: 2/19/2009 By MATTHEW PERRONEAP Business Writer WASHINGTON (AP) — Patients suffering from obsessive, distressing thoughts have a new treatment option: a pacemaker-like device that relieves anxiety with electrical jolts to the brain. The Food and Drug Administration on Thursday approved Medtronic’s Reclaim Deep Brain Stimulator device as the first..
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