FDA Adverse Event
Death
Summary report: N
BYRD DILATOR SHEATH SET, POLYPROPYLENE
MDR report key: 281139
·
Received June 7, 2000
Report
- Report Number
- 2522007-2000-00016
- Event Type
- Death
- Date Received
- June 7, 2000
- Date of Event
- May 27, 1999
- Report Date
- May 30, 2000
- Manufacturer
- COOK VASCULAR, INC.
- Product Code
- GCC
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
LEAD EXTRACTION PROCEDURE COMPLICATED BY HEMOTHORAX, INNOMINATE VEIN TEAR AND PT DEATH.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | BYRD DILATOR SHEATH SET, POLYPROPYLENE | CATHETER RETRIEVAL DEVICE | GCC | COOK VASCULAR, INC. | LR-PPLBES | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 43 YR | Death | LASER SHEATH. |