FDA Adverse Event
Summary report: N
*
MDR report key: 1233584
·
Received November 12, 2008
Report
- Report Number
- 1233584
- Date Received
- November 12, 2008
- Date of Event
- November 11, 2008
- Report Date
- November 12, 2008
- Manufacturer
- DEPUY ORTHOPAEDICS, INC.
- Product Code
- HTW
- Report Source
- User Facility report
- Reporter Location
- RI, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
DRILL BIT BROKE WHILE DRILLING THE ACETABULAR SCREWS. THE BIT WAS RETAINED IN ACETABULUM. NO HARM TO THE PT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | * | DRILL BIT, ORTHOPEDIC | HTW | DEPUY ORTHOPAEDICS, INC. | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 51 YR |