FDA Adverse Event
Injury
Summary report: N
UNK
MDR report key: 2946023
·
Received February 1, 2013
Report
- Report Number
- 2946023
- Event Type
- Injury
- Date Received
- February 1, 2013
- Date of Event
- September 19, 2012
- Report Date
- January 29, 2013
- Manufacturer
- UNK
- Product Code
- HWC
- Report Source
- User Facility report
- Reporter Location
- TX, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
TWO SCREWS FROM LEFT FOOT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 43771 | UNK | UNK | HWC | UNK | UNK | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 67 YR | Hospitalization |