FDA Adverse Event
Other
Summary report: N
CONTINUOUS EPIDURAL TRAY
MDR report key: 380376
·
Received March 6, 2002
Report
- Report Number
- 1217052-2002-00004
- Event Type
- Other
- Date Received
- March 6, 2002
- Date of Event
- February 4, 2002
- Report Date
- February 4, 2002
- Manufacturer
- PORTEX, INC.
- Product Code
- CAZ
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NY, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
THE USER STATES THEY EXPERIENCED PROBLEMS DURING PLACEMENT AND INADVERTENTLY SHEARED APPROX 3" OF THE CATHETER AGAINST THE NEEDLE BEVEL.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CONTINUOUS EPIDURAL TRAY | TRAY, ANESTHETIC CONDUCTION | CAZ | PORTEX, INC. | NA | K101789 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NO INFO | Other |