Model Number CI-1601-05 |
Device Problem
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 dizziness following initial implant surgery.Medication was prescribed (type unknown).It is believed that vertigo is not device related.Advanced bionics is in the process of obtaining additional information.When additional information is received, a supplemental report will be submitted.
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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.Additional information regarding treatment details were not provided.The medication prescribed was general medication from surgery.The recipient is doing well and dizziness resolved.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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