FDA Adverse Event
Injury
Summary report: N
UNK
MDR report key: 2945968
·
Received February 1, 2013
Report
- Report Number
- 2945968
- Event Type
- Injury
- Date Received
- February 1, 2013
- Date of Event
- January 7, 2013
- Report Date
- February 1, 2013
- Product Code
- HQX
- Report Source
- User Facility report
- Reporter Location
- TX, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
REMOVAL OR ORBITAL IMPLANT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 43851 | UNK | UNK | HQX | UNK | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 30 YR | Hospitalization |