FDA Adverse Event
Injury
Summary report: N
INTERTAN 10S NAILS
MDR report key: 3870689
·
Received June 12, 2014
Report
- Report Number
- 1020279-2014-00366
- Event Type
- Injury
- Date Received
- June 12, 2014
- Date of Event
- June 4, 2014
- Report Date
- June 4, 2014
- Manufacturer
- SMITH & NEPHEW, INC.
- Product Code
- JDS
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
.
Additional Manufacturer Narrative · 1
.
Description of Event or Problem · 1
IT WAS REPORTED A REVISION SURGERY WAS PERFORMED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 347919 | INTERTAN 10S NAILS | INTERTAN 11.5MM X 18CM 125D | JDS | SMITH & NEPHEW, INC. | 13JM08631 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Hospitalization| R | 71677110 LAG/COM SCREW KIT 110/105 LOT 10JM06764| 71645045 TRIGEN LPS LOT 13BM08108 |