FDA Adverse Event
Injury
Summary report: N
*
MDR report key: 38138
·
Received September 11, 1996
Report
- Report Number
- 1049753-1996-00003
- Event Type
- Injury
- Date Received
- September 11, 1996
- Date of Event
- July 18, 1996
- Product Code
- GBZ
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
DEVICE NOT IMPLICATED, EVENT ATTRIBUTED TO USER ERROR.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | * | GBZ |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |