FDA Adverse Event
Injury
Summary report: N
ODE
MDR report key: 317208
·
Received February 23, 2001
Report
- Report Number
- 1416900-2000-00061
- Event Type
- Injury
- Date Received
- February 23, 2001
- Date of Event
- August 1, 2000
- Report Date
- August 22, 2000
- Manufacturer
- BELTONE ELECTRONICS CORP.
- Product Code
- ESD
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MI, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
THE HEARING AID (H/A) DISPENSER REPORTED THAT THE USER EXPERIENCED AN EAR INFECTION POSSIBLY RELATED TO WEARING THE HEARING AID.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 7087 | ODE | HEARING AID | ESD | BELTONE ELECTRONICS CORP. | NA | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Life Threatening |