FDA Adverse Event Malfunction Summary report: N

2250051-2008-00093

MDR report key: 1003075 · Received February 11, 2008

Report

Report Number
2250051-2008-00093
Event Type
Malfunction
Date Received
February 11, 2008
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 PLUNGER CLAMP, TIP CLAMP, #2 POLE CABLE, AND TUBE LIFTER IN THE REPORTED PROBLEMS AREA OF THE PIPETTE ASSEMBLY. THE INSTRUMENT WAS 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