FDA Adverse Event
Injury
Summary report: N
R/T LOCK NAIL-FEM SE
MDR report key: 1973630
·
Received January 31, 2011
Report
- Report Number
- 1020279-2011-00019
- Event Type
- Injury
- Date Received
- January 31, 2011
- Report Date
- January 31, 2011
- Manufacturer
- SMITH & NEPHEW, INC.
- Product Code
- LXH
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CH
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IT WAS REPORTED THAT THE DEVICE COULD NOT BE INSTALLED AND DELAYED SURGERY 30-60 MINUTES.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | R/T LOCK NAIL-FEM SE | NAIL CAP | LXH | SMITH & NEPHEW, INC. | 07JM05130 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Hospitalization |