FDA Adverse Event
Malfunction
Summary report: N
AXSYM RUBELLA IGG ANTIBODY
MDR report key: 1152665
·
Received September 10, 2008
Report
- Report Number
- 1415939-2008-00258
- Event Type
- Malfunction
- Date Received
- September 10, 2008
- Date of Event
- April 9, 2008
- Report Date
- April 9, 2008
- Manufacturer
- ABBOTT LABORATORIES
- Product Code
- LFX
- PMA / PMN Number
- K954045
- Removal / Correction Number
- 1415939-6-06/08-004-C
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- LU
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THIS IS AN INITITAL REPORT. AN INVESTIGATION IS IN PROCESS. A FINAL REPORT WILL BE SUBMITTED WHEN THE INVESTIGATION IS COMPLETE.
Description of Event or Problem · 1
THE CUSTOMER STATED THAT THE AXSYM RUBELLA IGG REAGENT FAILED TO CALIBRATE WITH ERROR CODE 1018: CALIBRATION CHECK FAILURE, CAL A , RESULTS TOO HIGH, ON THE AXSYM ANALYZER. THE CUSTOMER PERFORMED ALL MAINTENANCE AND RECALIBRATED WITH ANOTHER REAGENT PACK WITH A NEW CALIBRATOR. THE CALIBRATION PASSED. NO IMPACT TO PT MGMT WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | AXSYM RUBELLA IGG ANTIBODY | MEIA FOR THE MEASUREMENT OF IGG ANTIBODY TO THE RUBELLA VIRUS | LFX | ABBOTT LABORATORIES | NA | 56659M200 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | AXSYM ANALYZER |