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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: COCHLEAR LTD NUCLEUS CI632 PROFILE PLUS WITH SLIM MODIOLAR ELECTRODE; NUCLEUS 24 COCHLEAR IMPLANT SYSTEM

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COCHLEAR LTD NUCLEUS CI632 PROFILE PLUS WITH SLIM MODIOLAR ELECTRODE; NUCLEUS 24 COCHLEAR IMPLANT SYSTEM Back to Search Results
Model Number CI632
Device Problem Appropriate Term/Code Not Available (3191)
Patient Problem Bacterial Infection (1735)
Event Type  Injury  
Event Description
Per the clinic, the patient experienced recurrent staphylococcus infection at the implant site which was treated with topical and oral antibiotics (specific date and duration not reported), however, the issue did not resolve.Subsequently, the device was explanted on (b)(6) 2023.There are plans to reimplant the patient with a new device; however, this has not occurred as of the date of this report.
 
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Brand Name
NUCLEUS CI632 PROFILE PLUS WITH SLIM MODIOLAR 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 Key18127912
MDR Text Key327989724
Report Number6000034-2023-03671
Device Sequence Number1
Product Code MCM
UDI-Device Identifier09321502036580
UDI-Public(01)09321502036580(11)230114(17)250113
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 11/14/2023,10/24/2023
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 Model NumberCI632
Was Device Available for Evaluation? No
Was the Report Sent to FDA? Yes
Date Report Sent to FDA11/14/2023
Distributor Facility Aware Date10/24/2023
Date Report to Manufacturer10/24/2023
Initial Date Manufacturer Received Not provided
Initial Date FDA Received11/13/2023
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
Patient SexFemale
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