Patients undergoing surgery could be at risk of injury or death from Monteris Medical Inc.'s NeuroBlate probe, part of the NeuroBlate System, according to US FDA. The agency announced it has known about the problem, in which the surgical tool has been reported to overheat, since October and now has designated it a high-risk class I recall.
"The FDA has received Medical Device Reports (MDRs) related to overheating of the probe, including one report of a patient who experienced an intracranial hemorrhage and died, although causality with...
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