FDA Adverse Event
Malfunction
Summary report: N
2250051-2007-00012
MDR report key: 830718
·
Received January 18, 2007
Report
- Report Number
- 2250051-2007-00012
- Event Type
- Malfunction
- Date Received
- January 18, 2007
- Product Code
- JTQ
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
THE INSTRUMENT HAS BEEN INVESTIGATED. THE FIELD SERVICE ENGINEER (FSE) EVALUATED THE INSTRUMENT AND FOUND A STUCK EJECT PIN IN THE PLUNGER CLAMP IN THE REPORTED PROBLEM AREA OF THE PIPETTE ASSEMBLY. THE INSTRUMENT WAS CLEANED, INSPECTED, TESTED, WITHOUT FURTHER PROBLEM, AND RETURNED TO SERVICE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | JTQ |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |