Model Number CI-1500-01 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Undesired Nerve Stimulation (1980)
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Event Date 02/01/2024 |
Event Type
Injury
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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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Event Description
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The recipient reportedly experienced improper device placement.The recipient presented with poor performance and facial nerve stimulation.Programming adjustments were made, however the issues did not resolve.The recipient ceased device use.The recipient's device was explanted.
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Manufacturer Narrative
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The recipient was reimplanted with another advanced bionics cochlear device.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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A review of the device history record was completed and no anomalies were noted. 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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