inforMED
MalfunctionCEO

PHOS2

Received Sep 22, 2023 · Event occurred Aug 29, 2023

Report 1823260-2023-03059 · MDR key 17798238

Device

Generic name

Phosphomolybdate (colorimetric), Inorganic Phosphorus

Manufacturer

Roche Diagnostics

Catalog number

03183793122

Lot number

70617701

Product problems

  • Incorrect Measurement
  • High Test Results
  • Non Reproducible Results
  • Incorrect Measurement
  • High Test Results
  • Non Reproducible Results

Patient

Unknown

  • No Clinical Signs, Symptoms or Conditions
  • No Clinical Signs, Symptoms or Conditions

Narrative

Additional Manufacturer Narrative

THE CUSTOMER DID NOT PERFORM THE WASH REACTION PART AND A SPECIAL WASH HAD TO BE IMPLEMENTED. PRODUCT LABELING STATES "PHOS2 ACTION REQUIRED SPECIAL WASH PROGRAMMING: THE USE OF SPECIAL WASH STEPS IS MANDATORY WHEN CERTAIN TEST COMBINATIONS ARE RUN TOGETHER ON COBAS INTEGRA ANALYZERS. REFER TO THE CLEAN METHOD SHEET FOR FURTHER INSTRUCTIONS AND FOR THE LATEST VERSION OF THE EXTRA WASH CYCLE LIST. WHERE REQUIRED, SPECIAL WASH/CARRY-OVER EVASION PROGRAMMING MUST BE IMPLEMENTED PRIOR TO REPORTING RESULTS WITH THIS TEST." THE CUSTOMER DID NOT PERFORM WEEKLY MAINTENANCE. PRODUCT LABELING STATES: "WEEKLY MAINTENANCE PERFORM THESE MAINTENANCE TASKS AT LEAST ONCE A WEEK. IN THIS SECTION: CLEANING THE CELL COVERS, CLEANING THE RINSE STATIONS, WASHING THE REACTION PARTS." THE INVESTIGATION REVIEWED THE CALIBRATION DATA; THE RESULTS WERE WITHIN SPECIFICATIONS. THE INVESTIGATION NOTED THAT THE RESULTS WERE IMPRECISE; THE RESULTS WERE OFTEN OUTSIDE THE SPECIFICATION OF +/-3 STANDARD DEVIATION (SD). THE FIELD SERVICE ENGINEER (FSE) STATED THAT THE EVENT WAS CAUSED BY THE SAMPLE PROBE THAT HAD TO BE REPLACED. PRODUCT LABELING STATES "REPLACING THE SAMPLE PROBE IF THE SAMPLE PROBE IS BENT OR OTHERWISE DAMAGED, YOU MUST REPLACE IT." THE INVESTIGATION DETERMINED THE EVENT WAS CONSISTENT WITH A PREANALYTIC ISSUE AT THE CUSTOMER SITE (THE SAMPLE PROBE HAD TO BE REPLACED). PREANALYTICS ARE WITHIN THE CUSTOMER'S RESPONSIBILITY. THE INVESTIGATION DID NOT IDENTIFY A PRODUCT PROBLEM.

Additional Manufacturer Narrative

THE SERIAL NUMBER OF THE CUSTOMER'S COBAS 4000 C311 STAND ALONE SYSTEM IS (B)(6). THE FIELD SERVICE ENGINEER (FSE) INSPECTED THE ANALYZER AND DETERMINED THAT THE SAMPLE PROBE HAD TO BE REPLACED AND A SPECIAL WASH HAD TO BE INSTALLED. THE INVESTIGATION IS ONGOING.

Description of Event or Problem

THE INITIAL REPORTER RECEIVED QUESTIONABLE PHOS2 PHOSPHATE (INORGANIC) VER.2 RESULTS FROM AN UNSPECIFIED NUMBER OF PATIENT SAMPLES TESTED ON THE COBAS 4000 C311 STAND ALONE SYSTEM. THE REPORTER STATED THAT THERE WERE NO ISSUES WITH THE PHOSPHATE ASSAY IF IT WAS RUN SEPARATELY. HOWEVER, WHEN IT WAS RUN WITH OTHER ASSAYS, THE RESULTS WOULD BE QUESTIONABLE AND HIGH. THE FIELD SERVICE REPRESENTATIVE (FSR) INSTRUCTED THE CUSTOMER TO CHANGE THE CELLS AND LAMP AND PERFORM CALIBRATION AND QC. THE ISSUE WAS NOT RESOLVED. IT WAS DETERMINED THAT THE WASH REACTION PART AND WEEKLY MAINTENANCE WERE NOT PERFORMED. THE TASKS WERE PERFORMED AND THE QC WAS ACCEPTABLE. HOWEVER, THE ISSUE WITH THE PATIENT RESULTS PERSISTED. THE REPORTER WAS ABLE TO PROVIDE ONE EXAMPLE OF DISCREPANT RESULTS: THE INITIAL RESULT WAS 4.11 MMOL/L. THE REPEAT RESULT WAS 1.03 MMOL/L.