FDA Adverse Event
Other
Summary report: N
VITAL-PORT
MDR report key: 253250
·
Received December 3, 1999
Report
- Report Number
- 2522007-1999-00028
- Event Type
- Other
- Date Received
- December 3, 1999
- Date of Event
- December 17, 1999
- Manufacturer
- COOK VASCULAR, INC.
- Product Code
- LJT
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- SZ
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
AS REPORTED TO THE DISTRIBUTOR BY THE PHYSICIAN, THE VITAL-PORT HAD A LEAKAGE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | VITAL-PORT Implant | VASCULAR ACCESS SYSTEM | LJT | COOK VASCULAR, INC. | 7129 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 3 YR | Other| R |