Model Number NEU_INS_STIMULATOR |
Device Problems
Insufficient Information (3190); Appropriate Term/Code Not Available (3191)
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Patient Problems
Therapeutic Response, Decreased (2271); No Known Impact Or Consequence To Patient (2692)
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Event Type
Injury
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Manufacturer Narrative
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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 with an implantable neurostimulator (ins).The patient stated that their ins just quit work ing so it was removed.They do not know why.There was a loss of therapy.The event date was unknown.The patient wanted their medical records so patient services redirected them to follow up with their healthcare professional (hcp).No further complications were reported/are anticipated.
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Manufacturer Narrative
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If information is provided in the future, a supplemental report will be issued.
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Search Alerts/Recalls
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