DIMENSION VISTA® CLINICAL CHEMISTRY SYSTEM
Report
- Report Number
- 9610806-2012-00008
- Event Type
- Malfunction
- Date Received
- August 1, 2012
- Date of Event
- June 20, 2012
- Report Date
- July 3, 2012
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
- Product Code
- CFQ
- PMA / PMN Number
- K990552
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CO, US
- Reporter Occupation
- MEDICAL TECHNOLOGIST
Narratives
ANALYSIS OF THE INSTRUMENT AND INSTRUMENT DATA INDICATE THAT THE CAUSE FOR THE FALSELY DEPRESSED IGA RESULTS IS UNKNOWN. THE DIMENSION VISTA(R) IGA FLEX(R) REAGENT CARTRIDGE IFU IN THE LIMITATIONS OF "PROCEDURE SECTION STATES: "THE IGA METHOD HAS BEEN DESIGNED TO MINIMIZE ANTIGEN EXCESS IN THE INITIAL SAMPLE DILUTION. HOWEVER, IT CQNNOT BE COMPLETELEY ELIMINATED AND IN RARE CASES VERY HIGH IMMUNOGLOBULIN CONCENTRATIONS MAY PRODUCE FALSELY-LOW RESULTS. MONOCLONAL IMMUNOGLOBULINS MAY SHOW REACTIVITY DIFFERENT FROM THE POLYCLONAL CALIBRATOR, WHICH IN ISOLATED CASES MAY LEAD TO ARTIFICIALLY DECREASED OR NON-LINEAR RESULTS." THE INSTRUMENT IS PERFORMING WITHIN SPECIFICATIONS. NO FURTHER EVALUATION OF THE DEVICE IS REQUIRED.
A SERIES OF FALSELY DEPRESSED IMMUNOGLOBULIN A (IGA) RESULTS WAS REPORTED ON A PATIENT'S SAMPLES. THE RESULTS WERE REPORTED TO THE PHYSICIAN. THE PATIENT WAS TESTED BY AN ALTERNATE METHODOLOGY (ELECTROPHORESIS) AND ELEVATED RESULTS WERE OBTAINED. THE ORIGINAL SAMPLES WERE RETESTED AND ELEVATED RESULTS WERE CONFIRMED. IT IS UNKNOWN IF PATIENT TREATMENT WAS ALTERED OR PRESCRIBED. THERE IS NO REPORT OF ADVERSE OUTCOME TO THE PATIENT AS A RESULT OF INITIAL FALSELY DEPRESSED IGA RESULTS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | DIMENSION VISTA® CLINICAL CHEMISTRY SYSTEM | IMMUNOGLOBULIN A FLEX® REAGENT CARTRIDGE | CFQ | SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH | 11195MA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |