Model Number CI-1400-01 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Tinnitus (2103); Vertigo (2134)
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Event Type
Injury
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Manufacturer Narrative
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Advanced bionics considers the investigation into this reportable event a closed.The recipient is reportedly doing better.The recipient will be monitored per center protocol.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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Event Description
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The recipient reportedly experienced vertigo and tinnitus.The recipient was reportedly prescribed medication for vertigo (type unknown).
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Manufacturer Narrative
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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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