FDA Adverse Event
Injury
Summary report: N
BAXTER SILICONE FOLEY CATHETER
MDR report key: 12822
·
Received April 18, 1994
Report
- Report Number
- 1483039-1994-00008
- Event Type
- Injury
- Date Received
- April 18, 1994
- Report Date
- April 5, 1994
- Manufacturer
- EUROMEDICAL
- Product Code
- KOD
- Adverse Event
- Yes
- Report Source
- Distributor report
- Reporter Location
- AL, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
CATHETER INSERTED INTO BOY AND WOULD NOT IRRIGATE. THE CATHETER WAS REMOVED SURGICALLY. THE CATHETER WAS REMOVED AND FOUND DEFECTIVE. THAT IS, NO FLUID WOULD MOVE THROUGH IT. NBO OTHER DETAILS PROVIDED AT THIS TIME.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | BAXTER SILICONE FOLEY CATHETER | CATHETER | KOD | EUROMEDICAL | NA | BOP070 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | Required Intervention |