It was reported the patient had a loss of therapeutic effect and their spasms had come back the day of this report.It had been a long time since the patient had checked the implantable neurostimulator (ins).The primary cell ins had lasted several years and the patient wanted to check the ¿lights.¿ the patient did not have any problems with their rechargeable ins.The patient had been battling lung cancer and their tremor had been horrible so they wanted to make sure the ins was working.When the patient checked the ins with the patient programmer, the green light next to the stimulation on was lit and the 9v battery was lit.There was no light next to the ins battery light.No interventions or outcome were reported regarding this event.Further follow-up is being conducted to obtain this information.If additional information is received, a follow up report will be sent.
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Concomitant products: product id 3387-40, lot # j0327188v, implanted: (b)(6) 2003, product type lead; product id 748251, serial # (b)(4), implanted: (b)(6) 2005, product type extension; product id 37642, serial # (b)(4), product type programmer, patient; product id 37651, serial # (b)(4), product type recharger; product id 37612, serial # (b)(4), implanted: (b)(6) 2013, product type implantable neurostimulator; product id 748251, serial # (b)(4), implanted: (b)(6) 2003, product type extension; product id 3387-40, lot # j0327188v, implanted: (b)(6) 2003, product type lead; product id 37612, serial # (b)(4), implanted: (b)(6) 2013, product type implantable neurostimulator.(b)(4).
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