Model Number NEU_INTERSTIM_INS |
Device Problems
Migration or Expulsion of Device (1395); Device Dislodged or Dislocated (2923)
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Patient Problem
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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The main component of the system and other applicable components are: product id: neu_unknown_lead, 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 consumer regarding a patient who was implanted with a neurostimulator for gastrointestinal/pelvic floor.It was reported that the patient's wire was replaced because it had moved.There were no further complications or anticipations reported with this event.[***refer to( b)(4) for information related to return of symptoms/worse at night***].
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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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