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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: COCHLEAR LTD NUCLEUS CI612 COCHLEAR IMPLANT WITH CONTOUR ADVANCE ELECTRODE; NUCLEUS 24 COCHLEAR IMPLANT SYSTEM

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COCHLEAR LTD NUCLEUS CI612 COCHLEAR IMPLANT WITH CONTOUR ADVANCE ELECTRODE; NUCLEUS 24 COCHLEAR IMPLANT SYSTEM Back to Search Results
Model Number CI612
Device Problem Positioning Failure (1158)
Patient Problem Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available (4581)
Event Date 04/04/2023
Event Type  Injury  
Event Description
Per the clinic, the tip of the electrode array was found to be folded over in the cochlea, resulting in the decision to explant the device.The device was explanted (b)(6) 2023, and the patient was reimplanted with another cochlear device during the same surgery.
 
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Brand Name
NUCLEUS CI612 COCHLEAR IMPLANT WITH CONTOUR ADVANCE ELECTRODE
Type of Device
NUCLEUS 24 COCHLEAR IMPLANT SYSTEM
Manufacturer (Section D)
COCHLEAR LTD
1 university avenue
macquarie university, nsw 2109
AS  2109
MDR Report Key18577375
MDR Text Key333658008
Report Number6000034-2024-00337
Device Sequence Number1
Product Code MCM
UDI-Device Identifier09321502036818
UDI-Public(01)09321502036818(11)210901(17)230831
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Distributor
Reporter Occupation Other
Type of Report Initial
Report Date 01/25/2024,01/05/2024
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Lay User/Patient
Device Expiration Date08/31/2023
Device Model NumberCI612
Was Device Available for Evaluation? No
Was the Report Sent to FDA? Yes
Date Report Sent to FDA01/25/2024
Distributor Facility Aware Date01/05/2024
Event Location Hospital
Date Report to Manufacturer01/05/2024
Initial Date Manufacturer Received Not provided
Initial Date FDA Received01/25/2024
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
Patient Age4 YR
Patient SexMale
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