FDA Adverse Event
Malfunction
Summary report: N
*
MDR report key: 1231666
·
Received August 1, 2008
Report
- Report Number
- 2250051-2008-00358
- Event Type
- Malfunction
- Date Received
- August 1, 2008
- Manufacturer
- *
- Product Code
- JTC
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
THE INSTRUMENT HAS BEEN INVESTIGATED. THE FIELD SERVICE ENGINEER (FSE) EVALUATED THE INSTRUMENT AND REPLACED PLUNGER #7 ALONG WITH LLD SPRING. THE INSTRUMENT WAS TESTED WITHOUT FURTHER PROBLEM, AND RETURNED TO EXPECTED OPERATION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | * | * | JTC | * | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |