Device 2 of 2.Reference mfr.Report# 3006705815-2018-00938: the patient is implanted with two leads and the manufacturer is unable to determine which lead is liable.It was reported the patient underwent an scs permanent implant procedure.During the procedure, the doctor was alerted that the patient experienced significant discomfort during the placement of the second of the two leads.The surgeon immediately re-positioned the needle and lead, and continued advancing the lead without issue.In post-op recovery the patient reported significant pain to the soles of the feet, the patient also had painful spasms down both legs.Therapy was left off till follow up and post op pain was reported to be receding at follow up.Therapy is providing 100 % relief to existing targeted pain.
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