FDA Adverse Event
Injury
Summary report: N
TRIUMPH I PORT
MDR report key: 41635
·
Received September 30, 1996
Report
- Report Number
- 1056436-1996-00059
- Event Type
- Injury
- Date Received
- September 30, 1996
- Date of Event
- August 28, 1996
- Report Date
- September 27, 1996
- Manufacturer
- HORIZON MEDICAL PRODUCTS INC.
- Product Code
- LJT
- Report Source
- Manufacturer report
- Reporter Location
- VA, US
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
MD REMOVED DEVICE (SURGICALLY) BECAUSE IT WAS NOT WORKING. NO FURTHER INFO IS AVAILABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TRIUMPH I PORT Implant | VASCULAR ACCESS SYSTEM | LJT | HORIZON MEDICAL PRODUCTS INC. | SSA-14-I | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 57 YR | Hospitalization| O |