FDA Adverse Event
Death
Summary report: N
MEDI. TECH BOSTON SCIENTIFIC CORP.
MDR report key: 207862
·
Received January 26, 1999
Report
- Report Number
- 207862
- Event Type
- Death
- Date Received
- January 26, 1999
- Date of Event
- January 24, 1999
- Report Date
- January 25, 1999
- Manufacturer
- MEDITECH BOSTON SCIENTIFIC CORP
- Product Code
- DTK
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- User Facility report
- Reporter Location
- MA, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
PT TO OPERATING ROOM FOR GREENFIELD VENA CAVA UMBRELLA. VENA CAVAL PERFORATION WHEN UMBRELLA DEPLOYED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MEDI. TECH BOSTON SCIENTIFIC CORP. Implant | TITANIUM GREENFIELD VENA CAVA FILTER | DTK | MEDITECH BOSTON SCIENTIFIC CORP | * | 275772 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 86 YR | Death |