FDA Adverse Event
Injury
Summary report: N
ACUTRAK CANNULATED DRILL
MDR report key: 384996
·
Received March 25, 2002
Report
- Report Number
- 3025141-2000-00001
- Event Type
- Injury
- Date Received
- March 25, 2002
- Date of Event
- July 18, 2000
- Report Date
- March 23, 2002
- Manufacturer
- ACUMED, INC.
- Product Code
- HTW
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
DURING AN ACUTRAK SURGERY, THE DRILL TIP BROKE OFF AND WAS LEFT IN THE PATIENT. THE SURGERY WAS COMPLETED SUCCESSFULLY WITH K-WIRES.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ACUTRAK CANNULATED DRILL | SURGICAL INSTRUMENT | HTW | ACUMED, INC. | AT-7032 | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Other |