Model Number CI622 |
Device Problems
No Apparent Adverse Event (3189); Insufficient Information (3190)
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Patient Problems
Insufficient Information (4580); No Clinical Signs, Symptoms or Conditions (4582)
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Event Type
Injury
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Manufacturer Narrative
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This report is submitted on february 19, 2024.
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Event Description
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Per the clinic, the device was explanted (date not reported) for unspecified medical reasons.Additional information has been requested but has not been made available as of the date of this report.
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Manufacturer Narrative
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Correction: the previous or initial mdr submitted on february 19, 2024, was filed inadvertently.Adverse event is not related to cochlear device.This report is submitted on march 21, 2024.
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Search Alerts/Recalls
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