Model Number CI-1500-04 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Pain (1994); Dizziness (2194)
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Event Type
Injury
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Manufacturer Narrative
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Disclaimer: advanced bionics does not intend that this report be any admission of liability, fault or product defect.
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Event Description
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The recipient is reportedly experiencing pain and non auditory sensations with and without device use.Antibiotics (type unknown), paracetamol and morphine were administered, however the issue did not resolve.There is no evidence of infection.Programming adjustments have been made.
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Manufacturer Narrative
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The recipient is reportedly experiencing dizziness.The recipient was prescribed gabapentin for pain.Disclaimer: advanced bionics does not intend that this report be any admission of liability, fault or product defect.
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Manufacturer Narrative
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Disclaimer: advanced bionics does not intend that this report be any admission of liability, fault or product defect.
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Manufacturer Narrative
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Advanced bionics considers the investigation into this reportable event as closed.The recipient's pain has reduced and dizziness has resolved.The recipient has resumed device use.No further details will be provided.This is the final report.Disclaimer: advanced bionics does not intend that this report be any admission of liability, fault or product defect.
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Search Alerts/Recalls
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