FDA Adverse Event
Injury
Summary report: N
INTERTAN NAILS
MDR report key: 2970287
·
Received February 20, 2013
Report
- Report Number
- 1020279-2013-00110
- Event Type
- Injury
- Date Received
- February 20, 2013
- Date of Event
- February 15, 2013
- Report Date
- February 15, 2013
- Manufacturer
- SMITH & NEPHEW, INC.
- Product Code
- JDS
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IT WAS REPORTED WHILE ENGAGING\DISENGAGING THE DEVICE INTRA-OPERATIVELY, THERE WAS A DELAY OF SURGERY TIME.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 73133 | INTERTAN NAILS | 10MM X 18CM 125D | JDS | SMITH & NEPHEW, INC. | 12LM02552 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 80 YR | Hospitalization| R |