DIMENSION VISTA® CLINICAL CHEMISTRY SYSTEM
Report
- Report Number
- 2517506-2013-00050
- Event Type
- Malfunction
- Date Received
- March 7, 2013
- Date of Event
- December 8, 2012
- Report Date
- February 14, 2013
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW
- Product Code
- KXT
- PMA / PMN Number
- K093441
- Removal / Correction Number
- 2517506-03-06-2013-003-C
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- VA, US
- Reporter Occupation
- MEDICAL TECHNOLOGIST
Narratives
SIEMENS HEALTHCARE DIAGNOSTICS INC. HAS CONFIRMED CUSTOMER COMPLAINTS OF LOW QC AND PATIENT RECOVERY FOR DIGOXIN WHEN THIS CALIBRATOR LOT IS USED TO CALIBRATE THE DIGXN METHOD. INTERNAL TESTING HAS CONFIRMED AN AVERAGE 15% LOW BIAS IN THE THERAPEUTIC RANGE OF 0.9 TO 2.0 NG/ML. THE CAUSE OF THE BIAS LOW IN DIGOXIN RECOVERIES IS CALIBRATOR INACCURACY. SIEMENS HEALTHCARE DIAGNOSTICS INC. CONDUCTED A VOLUNTARY RECALL FOR DIMENSION VISTA DRUG 4 CAL (KC460) LOT 2KD052 AND DRUG 4 CAL (KC460A) LOT 2KD053. AN URGENT MEDICAL DEVICE RECALL, COMMUNICATION #13-13, WAS ISSUED IN FEBRUARY 2013 TO IMPACTED CUSTOMERS. CUSTOMERS WERE INSTRUCTED TO IMMEDIATELY DISCONTINUE USE AND TO DISCARD ANY REMAINING INVENTORY OF DIMENSION VISTA DRUG 4 CAL (KC460) LOT 2KD052 AND DRUG 4 CAL (KC460A) LOT 2KD053.
BIASED LOW DIGOXIN RESULTS WERE OBTAINED ON QC AND PATIENT SAMPLES AFTER CALIBRATION. PATIENT RESULTS WERE REPORTED TO THE PHYSICIAN. IT IS UNKNOWN IF PATIENT TREATMENT WAS ALTERED OR PRESCRIBED AS A RESULT OF THE BIASED LOW DIGOXIN RESULTS. THERE WAS NO REPORT OF ADVERSE HEALTH CONSEQUENCES AS A RESULT OF THE BIASED LOW DIGOXIN RESULTS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 98297 | DIMENSION VISTA® CLINICAL CHEMISTRY SYSTEM | DRUG 4 CALIBRATOR | KXT | SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW | 2KD052 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |