inforMED
MalfunctionPSZ

KIT FLU VERITOR SYSTEM 30 TEST JAPAN

Received Jul 23, 2025 · Event occurred Sep 25, 2024

Report 3006948883-2025-00321 · MDR key 22575959

Device

Generic name

Devices Detecting Influenza A, B, And C Virus Antigens

Catalog number

256052

Lot number

UNKNOWN

Product problems

  • Incorrect, Inadequate or Imprecise Result or Readings
  • Incorrect, Inadequate or Imprecise Result or Readings

Patient

NA · Unknown

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

Narrative

Description of Event or Problem

IT WAS REPORTED WHILE TESTING WITH KIT FLU VERITOR SYSTEM 30 TEST JAPAN, THERE WAS A CRACK ON THE TEST CARTRIDGE WHICH WAS VISUALLY INTERPRETED AS A POSITIVE. THE TEST WAS REPEATED WITH THE SAME SAMPLE AND THE RESULT WAS NEGATIVE. THERE WERE NO HEALTH IMPACT OR CONSEQUENCES REPORTED.

Additional Manufacturer Narrative

E.1 INITIAL REPORTER FACILITY NAME: (B)(6). INVESTIGATION SUMMARY THIS STATEMENT SUMMARIZES THE INVESTIGATION RESULTS REGARDING A COMPLAINT THAT ALLEGES FALSE POSITIVE WHEN USING KIT FLU VERITOR SYSTEM 30 TEST JAPAN (MATERIAL#: 256052), BATCH NUMBER UNKNOWN. THE CUSTOMER REPORTED THAT THERE WAS A THIN LINE-LIKE CRACK THAT WAS OBSERVED ON THE A LINE OF THE TEST CARTRIDGE, WHICH WAS READ AS POSITIVE. THE SAME EXTRACT WAS INOCULATED ONTO ANOTHER CARTRIDGE THAT THEN GAVE A NEGATIVE RESULT. BD QUALITY PERFORMS A SYSTEMATIC APPROACH TO INVESTIGATE ALL COMPLAINTS. THIS APPROACH INVOLVES REVIEW OF MANUFACTURING BATCH HISTORY RECORDS, VISUAL INSPECTION OF RETENTION SAMPLES, AND VISUAL INSPECTION OF CUSTOMER RETURNED SAMPLES, IF APPLICABLE. BATCH HISTORY RECORD (BHR) REVIEW AND RETAIN SAMPLE TESTING WERE NOT PERFORMED AS THERE WAS NO BATCH NUMBER PROVIDED. NO SAMPLES WERE RECEIVED; THEREFORE, RETURN SAMPLE ANALYSIS COULD NOT BE PERFORMED. FROM THE 4 PHOTOS PROVIDED, 1 PHOTO SHOWS 4 DEVICES WITH AN EXTREMELY FAINT LINE AROUND COLUMN A. IT IS DIFFICULT TO DISTINGUISH WHETHER IT IS A LINE OR A SCRATCH. SINCE NO PHOTOS OF THE VERITOR ANALYZER RESULTS WERE RETURNED, WE ARE UNABLE TO CONFIRM THE COMPLAINT THROUGH THE PROVIDED PHOTOS. A TREND ANALYSIS FOR FALSE POSITIVE WAS CONDUCTED, NO ADVERSE TREND WAS IDENTIFIED. THERE WERE NO CORRECTIVE ACTIONS TAKEN AT THIS TIME. THIS MDR IS BEING SUBMITTED AS PART OF A RETROSPECTIVE REVIEW OF RECORDS DATING APRIL 2023¿2025, UNDER CAPA 11910483.