FDA Adverse Event
Injury
Summary report: N
UNK
MDR report key: 125934
·
Received October 10, 1997
Report
- Report Number
- 125934
- Event Type
- Injury
- Date Received
- October 10, 1997
- Date of Event
- September 30, 1997
- Report Date
- October 7, 1997
- Manufacturer
- UNK
- Product Code
- LPW
- Adverse Event
- Yes
- Report Source
- User Facility report
- Reporter Location
- PA, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
DURING ABDOMINAL SURGERY FOR TREATMENT OF AN ABSCESS, THE BLADDER WAS PERFORATED. THE SURGEON REPAIRED THE PERFORATION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | UNK | METZENBAUM SCISSORS | LPW | UNK | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 65 YR | Required Intervention |