Model Number SONATA |
Device Problem
Output Problem (3005)
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Patient Problem
Failure of Implant (1924)
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Event Type
Injury
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Manufacturer Narrative
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The device has not been explanted.If it should be explanted, it is to be returned to the manufacturer for evaluation.When available, a device failure analysis will be submitted as a follow up report.
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Event Description
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In situ testing showed affected channels.No decline in hearing performance with the device has been noticed.
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Event Description
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In situ testing showed affected channels.No decline in hearing performance with the device has been noticed.Re-implantation has been recommended.However, no date has been scheduled yet.
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Manufacturer Narrative
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Additional information: according to the currently available information, damage to the active electrode, as it might be caused by an external mechanical impact appears likely.However to confirm an exact root cause of failure a device investigation of the explanted device is necessary.No date for revision surgery has been set yet.
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Event Description
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In situ testing showed affected channels.No decline in hearing performance with the device has been noticed.The user was re-implanted.Despite requested, the concerned device could not be retrieved for investigation yet.
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Manufacturer Narrative
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Additional information: according to the currently available information, damage to the active electrode, as it might be caused by an external mechanical impact appears likely.However to confirm an exact root cause of failure a device investigation of the explanted device is necessary.The concerned device was explanted but has not been received for investigation yet.
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Event Description
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In situ testing showed affected channels.No decline in hearing performance with the device has been noticed.The user was re-implanted.
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Manufacturer Narrative
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Conclusion: overload fractures in the active electrode which are consistent with an external mechanical impact were determined to be the root cause of device failure.The active electrode also showed some additional damage to the electrode wires, as being caused by minute device mobility.An accident or impact might have weakened the fixation of the implant, consequently leading to electrode mobility.The problems given in the recipient report appear to match the damage found.This is a final report.
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Search Alerts/Recalls
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