FDA Adverse Event
Summary report: N
CATHETER, 4.0 FR
MDR report key: 10649
·
Received December 23, 1993
Report
- Report Number
- MW1000219
- Date Received
- December 23, 1993
- Report Date
- December 22, 1993
- Manufacturer
- AMERICAN CATHETER CORP.
- Product Code
- FFL
- Report Source
- Voluntary report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
THE STONE BASKET WAS FOUND TO BE BENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CATHETER, 4.0 FR | FFL | AMERICAN CATHETER CORP. | 709316 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |