FDA Adverse Event
Malfunction
Summary report: N
5221738
MDR report key: 5221738
·
Received November 13, 2015
Report
- Report Number
- 5221738
- Event Type
- Malfunction
- Date Received
- November 13, 2015
- Date of Event
- October 9, 2015
- Report Date
- November 11, 2015
- Adverse Event
- Yes
- Report Source
- User Facility report
- Reporter Location
- MO, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
WHILE IN USE, THE PRODUCT STOPPED. IT WAS FELT TO BE RELATED TO THE BATTERY LIFE.
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 21 YR |