FDA Adverse Event
Summary report: N
*
MDR report key: 2496932
·
Received February 3, 2012
Report
- Report Number
- 2496932
- Date Received
- February 3, 2012
- Date of Event
- September 27, 2011
- Report Date
- February 3, 2012
- Manufacturer
- ACUMED
- Product Code
- HTY
- Report Source
- User Facility report
- Reporter Location
- KY, US
Narratives
Description of Event or Problem · 1
TIP OF K-WIRE BROKE OFF IN PATIENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | * | K-WIRE | HTY | ACUMED | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 51 YR |