FDA Adverse Event
Malfunction
Summary report: N
BBL VACUTAINER
MDR report key: 2862304
·
Received December 3, 2012
Report
- Report Number
- 2862304
- Event Type
- Malfunction
- Date Received
- December 3, 2012
- Date of Event
- November 30, 2012
- Report Date
- December 3, 2012
- Manufacturer
- BECTON DICKINSON
- Product Code
- JTX
- Product Problem
- Yes
- Report Source
- User Facility report
- Reporter Location
- CO, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
THREE OF THE ANAEROBIC SPECIMEN TUBES BROKE DURING NORMAL USE. ALSO, IT APPEARED THERE WAS MOISTURE INSIDE THE TUBES.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | BBL VACUTAINER | TRANSPORT SYSTEMS, ANAEROBIC | JTX | BECTON DICKINSON | * | 2061411 | |
| 2 | BBL VACUTAINER | TRANSPORT SYSTEMS, ANAEROBIC | JTX | BECTON DICKINSON | * | 2146020 | |
| 3 | BBL VACUTAINER | TRANSPORT SYSTEMS, ANAEROBIC | JTX | BECTON DICKINSON | * | 1242294 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |