FDA Adverse Event
Injury
Summary report: N
SMART SET MV - BONE CEMENT
MDR report key: 2574892
·
Received April 9, 2012
Report
- Report Number
- MW5025360
- Event Type
- Injury
- Date Received
- April 9, 2012
- Date of Event
- October 29, 2009
- Manufacturer
- DEPUY
- Product Code
- LOD
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- IL, US
- Reporter Occupation
- BIOMEDICAL ENGINEER
Narratives
Description of Event or Problem · 1
ON (B)(6) 2009, BILATERAL TOTAL KNEE ARTHROPLASTY FOR DJD OF BOTH KNEES. ON (B)(6) 2011, REVISION OF TIBIAL COMPONENT, RIGHT KNEE DUE TO LOOSE TIBIAL COMPONENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SMART SET MV - BONE CEMENT | BONE CEMENT | LOD | DEPUY | 2946615 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 59 YR | Required Intervention |