FDA Adverse Event
Death
Summary report: N
SCHNEIDER WALLSTENT TRACHEOBRONCHIAL PROSTHESIS
MDR report key: 182494
·
Received August 12, 1998
Report
- Report Number
- 2183541-1998-00033
- Event Type
- Death
- Date Received
- August 12, 1998
- Date of Event
- July 14, 1998
- Report Date
- August 12, 1998
- Manufacturer
- SCHNEIDER (USA) PERIPHERAL DIV.
- Product Code
- JCT
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- KS, US
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
A REPORT REGARDING THIS EVENT WAS SUBSEQUENTLY OBTAINED ON 8/21/1998.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SCHNEIDER WALLSTENT TRACHEOBRONCHIAL PROSTHESIS Implant | TRANSHEPATIC BIL./TRACH-BRONCH | JCT | SCHNEIDER (USA) PERIPHERAL DIV. | B16609110 | 9601501 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NO INFO | Death |