Model Number CI-1601-04 |
Device Problems
Defective Device (2588); Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Dizziness (2194)
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Event Type
Injury
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Event Description
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The recipient is reportedly experiencing poor performance.Programming adjustments were made, however, the issue did not resolve.The recipient was prescribed steroids for reported dizziness following implant surgery.Revision surgery will be scheduled.
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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 will reportedly not pursue revision surgery at this time.The recipient is wearing the device.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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