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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 CI612
Device Problem Appropriate Term/Code Not Available (3191)
Patient Problems Facial Nerve Paralysis (1846); Pain (1994); Dizziness (2194)
Event Date 05/20/2020
Event Type  Injury  
Manufacturer Narrative
This report is submitted on june 15, 2020.
 
Event Description
Per the audiologist, the patient was experiencing facial paralysis, dizziness and shooting pain in her jaw 1 week after implantation.The device was explanted on (b)(6) 2020.The patient was reimplanted with a new device during the same surgery.
 
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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, 2109
AS  2109
MDR Report Key10151657
MDR Text Key195077418
Report Number6000034-2020-01495
Device Sequence Number1
Product Code MCM
UDI-Device Identifier09321502036818
UDI-Public(01)09321502036818(11)191128(17)211127
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Distributor
Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date 06/15/2020,05/21/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received06/14/2020
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Lay User/Patient
Device Expiration Date11/27/2021
Device Model NumberCI612
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? Yes
Date Report Sent to FDA06/15/2020
Date Report to Manufacturer05/21/2020
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage N
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
Patient Age41 YR
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