FDA Adverse Event
Injury
Summary report: N
BCS TIBIA BASE PLATE
MDR report key: 3092638
·
Received May 3, 2013
Report
- Report Number
- 1020279-2013-00247
- Event Type
- Injury
- Date Received
- May 3, 2013
- Date of Event
- December 23, 2012
- Report Date
- April 23, 2013
- Manufacturer
- SMITH & NEPHEW, INC.
- Product Code
- JWH
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
.
Description of Event or Problem · 1
PATIENT WAS ADMITTED INTO THE HOSPITAL FOR BLEEDING.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 193951 | BCS TIBIA BASE PLATE | JOURNEY TIBIA BASE NP LT SZ 5 | JWH | SMITH & NEPHEW, INC. | 12EM04573 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 63 YR | Hospitalization | 71332535/12GM01806| 74027262/12AM10967| 74024838/12FM00231| 74022125/12EM00472| 71332535/12HM12059 |