MAUDE Adverse Event Report: COCHLEAR LTD CP1150 MAGNET (STRENGTH 4 (I)); NUCLEUS 24 COCHLEAR IMPLANT SYSTEM

Model Number CP1150

Device Problem Insufficient Information (3190)

Patient Problems Unspecified Infection (1930); Skin Inflammation/ Irritation (4545)

Event Type  Injury  

Event Description

Per the clinic, the patient experienced an infection and skin irritation at the magnet site (date not reported).Additional information has been requested but it has not been made available as of the date of this report.

• Brand Name: CP1150 MAGNET (STRENGTH 4 (I))
• Type of Device: NUCLEUS 24 COCHLEAR IMPLANT SYSTEM
• Manufacturer (Section D): COCHLEAR LTD; 1 university avenue; macquarie university, nsw 2109 ; AS 2109
• MDR Report Key: 19068755
• MDR Text Key: 339667429
• Report Number: 6000034-2024-01377
• Device Sequence Number: 1
• Product Code: MCM
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Distributor
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 04/09/2024,03/20/2024

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 Model Number: CP1150
• Device Catalogue Number: P1540175
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: Yes
• Date Report Sent to FDA: 04/09/2024
• Distributor Facility Aware Date: 03/20/2024
• Event Location: Hospital
• Date Report to Manufacturer: 03/20/2024
• Initial Date Manufacturer Received: Not provided
• Initial Date FDA Received: 04/08/2024
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention
• Patient Sex: Female