FDA Adverse Event
Malfunction
Summary report: N
CLARION
MDR report key: 2063799
·
Received April 6, 2011
Report
- Report Number
- 3006556115-2011-00145
- Event Type
- Malfunction
- Date Received
- April 6, 2011
- Date of Event
- March 16, 2011
- Report Date
- March 16, 2011
- Manufacturer
- ADVANCED BIONICS LLC
- Product Code
- MCM
- PMA / PMN Number
- P960058
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- SP
- Reporter Occupation
- HEALTH PROFESSIONAL
Narratives
Description of Event or Problem · 1
THE PATIENT REPORTEDLY EXPERIENCED A LOSS OF LOCK WITH HER INTERNAL DEVICE. SURGERY TO EXPLANT THE PATIENT'S DEVICE WILL BE SCHEDULED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CLARION | COCHLEAR IMPLANT | MCM | ADVANCED BIONICS LLC | AB-5100R | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 13 YR |