Model Number CI-1601-04 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
|
Patient Problem
Tinnitus (2103)
|
Event Type
Injury
|
Manufacturer Narrative
|
Disclaimer: advanced bionics does not intend that this report be any admission of liability, fault or product defect.
|
|
Event Description
|
The recipient is reportedly experiencing tinnitus.Programming adjustments have been made, however the issue did not resolve.The recipient was prescribed steroids.
|
|
Manufacturer Narrative
|
The recipient was reportedly prescribed another medication (type unknown), however the issue did not resolve.Disclaimer: advanced bionics does not intend that this report be any admission of liability, fault or product defect.
|
|
Search Alerts/Recalls
|