Model Number NEU_INS_STIMULATOR |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Unspecified Infection (1930); Numbness (2415); Insufficient Information (4580)
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Event Type
Injury
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Manufacturer Narrative
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Concomitant medical products: product id: neu_unknown_lead, serial#: unknown.Product type: lead.If information is provided in the future, a supplemental report will be issued.
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Event Description
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Information was received from a patient regarding their implantable neurostimulator (ins).It was reported that patient had neuro stim in their back years ago; had to have it removed due to worse numbness infection toes and legs giving out/ still to this day have problems with legs and feet.Also they left wires in back so can't get mris.
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Search Alerts/Recalls
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