FDA Adverse Event
Injury
Summary report: N
2250051-2006-00254
MDR report key: 742734
·
Received June 6, 2006
Report
- Report Number
- 2250051-2006-00254
- Event Type
- Injury
- Date Received
- June 6, 2006
- 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 THE TIP 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 | JTC |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |