FDA Adverse Event
Injury
Summary report: N
SYSTEM JO
MDR report key: 6309615
·
Received February 7, 2017
Report
- Report Number
- 1032263-2017-00004
- Event Type
- Injury
- Date Received
- February 7, 2017
- Date of Event
- May 20, 2016
- Report Date
- February 7, 2017
- Manufacturer
- UNITED CONSORTIUM
- Product Code
- NUC
- PMA / PMN Number
- K150480
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
USED ONCE AND EXPERIENCED A BURNING SENSATION AND DISCHARGE FOR A NUMBER OF DAYS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 91593 | SYSTEM JO | PERSONAL LUBRICANT | NUC | UNITED CONSORTIUM | 40034 | 4146 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |