FDA Adverse Event
Malfunction
Summary report: N
THORACIC SILICONE CATHETER 32 FR.
MDR report key: 186392
·
Received September 3, 1998
Report
- Report Number
- 2020735-1998-00002
- Event Type
- Malfunction
- Date Received
- September 3, 1998
- Date of Event
- July 31, 1998
- Report Date
- September 3, 1998
- Manufacturer
- AXIOM MEDICAL, INC.
- Product Code
- KDQ
- Report Source
- Manufacturer report
Narratives
Description of Event or Problem · 1
BASED ON THE CURRENT INFO PROVIDED BY THE HOSP, THE PT WAS DISCHARGED ON 8/3/98 IN STABLE CONDITION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | THORACIC SILICONE CATHETER 32 FR. | KDQ | AXIOM MEDICAL, INC. | 111132 OR 111132AT | UNCERTAIN |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |