COBAS 6000 C501 MODULE
Received Oct 12, 2010 · Event occurred Sep 20, 2010
Report 1823260-2010-06064 · MDR key 1864575
Device
Generic name
Clinical Chemistry Analyzer
Manufacturer
Roche DiagnosticsModel number
NACatalog number
05036453001
Lot number
NA
Product problems
- Low Test Results
Patient
Not reported
- No Known Impact Or Consequence To Patient
Narrative
Description of Event or Problem
A CUSTOMER RECEIVED QUESTIONABLE RESULTS FOR MULTIPLE ASSAYS WHEN TESTING FOUR PATIENT SAMPLES. RESULTS FOR THREE OF THE PATIENTS WERE DISCREPANT. PATIENT 1, NEWBORN: THE INITIAL GLUCOSE RESULT WAS 7 MG/DL. THE SAMPLE REPEATED ON A DIFFERENT ANALYZER (SERIAL NUMBER UNKNOWN) GAVE 135 MG/DL. THE INITIAL ALKALINE PHOSPHATASE RESULT WAS 6 U/L. THE SAMPLE REPEATED ON A DIFFERENT ANALYZER (SERIAL NUMBER UNKNOWN) GAVE 57 U/L. THE INITIAL TOTAL PROTEIN RESULT WAS 0.4 G/DL. THE SAMPLE REPEATED ON A DIFFERENT ANALYZER (SERIAL NUMBER UNKNOWN) GAVE 6.6 G/DL. PATIENT 2, FEMALE NEWBORN: THE INITIAL CO2 RESULT WAS 19 MMOL/L. THE SAMPLE REPEATED ON A DIFFERENT ANALYZER (SERIAL NUMBER UNKNOWN) GAVE 28 MMOL/L. THE INITIAL TOTAL PROTEIN RESULT WAS 1.4 G/DL. THE SAMPLE REPEATED ON A DIFFERENT ANALYZER (SERIAL NUMBER UNKNOWN) GAVE 4.1 G/DL. THE INITIAL GLUCOSE RESULT WAS 44 MG/DL. THE SAMPLE REPEATED ON A DIFFERENT ANALYZER (SERIAL NUMBER UNKNOWN) GAVE 71 MG/DL. THE INITIAL TOTAL BILIRUBIN RESULT WAS 2.1 MG/DL. THE SAMPLE REPEATED ON A DIFFERENT ANALYZER (SERIAL NUMBER UNKNOWN) GAVE 7.2 MG/DL. THE INITIAL ALKALINE PHOSPHATASE RESULT WAS 200 U/L. THE SAMPLE REPEATED ON A DIFFERENT ANALYZER (SERIAL NUMBER UNKNOWN) GAVE 571 U/L. THE INITIAL PHOSPHORUS RESULT WAS 1.5 MG/DL. THE SAMPLE REPEATED ON A DIFFERENT ANALYZER (SERIAL NUMBER UNKNOWN) GAVE 4.7 MG/DL. PATIENT 3, MALE NEWBORN: THE INITIAL TOTAL BILIRUBIN RESULT WAS 0.2 MG/DL. THE SAMPLE REPEATED ON THE SAME ANALYZER GAVE 8.8 MG/DL. THE ONLY INITIAL RESULTS REPORTED OUTSIDE THE LABORATORY WERE THE TOTAL BILIRUBIN RESULTS FOR PATIENT 3. THE CUSTOMER HAD NOT BEEN INFORMED OF ANY TREATMENT PROVIDED, ALTERED OR WITHHELD DUE TO THE INITIAL RESULTS. NO ADVERSE EVENTS WERE REPORTED. REAGENT LOT NUMBERS: CO2 628042 TOTAL PROTEIN 631380 GLUCOSE 625902 TOTAL BILIRUBIN 62872801 ALKALINE PHOSPHATASE 62762601 PHOSPHORUS 627979 THE FIELD SERVICE REPRESENTATIVE WAS UNABLE TO REPRODUCE THE ERRONEOUS RESULTS OR DETERMINE A CAUSE. HE INSPECTED INSTRUMENT SAMPLING AND CUVETTE RINSE FUNCTIONS AS A PREVENTIVE MEASURE. THE CUSTOMER RAN PRECISION AND QUALITY CONTROL ON ALL TESTS INVOLVED AND THE RESULTS WERE WITHIN SPECIFICATION.