FDA Adverse Event
Injury
Summary report: N
CONTIPLEX TUOHY CONTINUOUS NBS
MDR report key: 3983498
·
Received August 1, 2014
Report
- Report Number
- MW5037615
- Event Type
- Injury
- Date Received
- August 1, 2014
- Date of Event
- July 1, 2014
- Report Date
- July 31, 2014
- Manufacturer
- BRAUN
- Product Code
- OGE
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- VT, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
NERVE BLOCK CATHETER KINKED AND CLOTTED OFF DURING INSERTION BY ANESTHESIOLOGIST. DIAGNOSIS OR REASON FOR USE: NERVE BLOCK FOR ORTHO SURGERY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 451538 | CONTIPLEX TUOHY CONTINUOUS NBS | NERVE BLOCK SET | OGE | BRAUN | CONTIPLEX TUOHY CONTINUOUS NBS | 61353241 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 58 YR | Required Intervention |