FDA Adverse Event
Summary report: N
BD
MDR report key: 1003930
·
Received January 30, 2008
Report
- Report Number
- 1003930
- Date Received
- January 30, 2008
- Date of Event
- January 11, 2008
- Report Date
- January 30, 2008
- Manufacturer
- BECTON DICKINSON
- Product Code
- BSP
- Report Source
- User Facility report
- Reporter Location
- VT, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
HUB OF ASPIRATION NEEDLE BROKE WHEN DOCTOR WAS DOING ASPIRATION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | BD | NEEDLE, SPINAL | BSP | BECTON DICKINSON | * | 3104643 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 78 YR |