FDA Adverse Event
Injury
Summary report: N
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
MDR report key: 3222678
·
Received July 12, 2013
Report
- Report Number
- 6000034-2013-01231
- Event Type
- Injury
- Date Received
- July 12, 2013
- Date of Event
- June 25, 2013
- Report Date
- October 10, 2013
- Manufacturer
- COCHLEAR LTD
- Product Code
- MCM
- PMA / PMN Number
- 970051
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- AUDIOLOGIST
Narratives
Additional Manufacturer Narrative · 1
(B)(4).
Additional Manufacturer Narrative · 1
THIS REPORT IS FILED DECEMBER 13, 2013.
Description of Event or Problem · 1
PER THE CLINIC, THE PATIENT REQUESTED THAT THE DEVICE BE EXPLANTED DUE TO REPORTED LACK OF BENEFIT FROM THE DEVICE AND INTERNAL COIL EXPOSURE. THE DEVICE WAS EXPLANTED (B)(6), 2013; IT IS UNKNOWN IF THERE ARE PLANS TO REIMPLANT THE PATIENT AS OF THE DATE OF THIS REPORT, (B)(6), 2013.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 321917 | NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM | MCM, PRODUCT CODE: MCM | MCM | COCHLEAR LTD | CI24RE (CA) |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 89 YR | Required Intervention |