FDA Adverse Event
Injury
Summary report: N
UNK
MDR report key: 1013896
·
Received March 11, 2008
Report
- Report Number
- 1013896
- Event Type
- Injury
- Date Received
- March 11, 2008
- Date of Event
- July 11, 2007
- Report Date
- March 7, 2008
- Manufacturer
- INAMD
- Product Code
- FWM
- Adverse Event
- Yes
- Report Source
- User Facility report
- Reporter Location
- HI, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
INFECTED IMPLANT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | UNK | BREAST IMPLANT | FWM | INAMD | NA | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 61 YR | Hospitalization |