BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD RAPID DETECTION OF SARS-COV-2 VERITOR

    MDR report key: 10803461 · Received November 6, 2020

    Report

    Report Number
    1119779-2020-00929
    Event Type
    Malfunction
    Date Received
    November 6, 2020
    Date of Event
    October 26, 2020
    Report Date
    September 8, 2021
    Manufacturer
    BECTON, DICKINSON & CO. (SPARKS)
    Product Code
    QKP
    PMA / PMN Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 0

    INVESTIGATION SUMMARY: THIS MEMO IS TO SUMMARIZE THE INVESTIGATION RESULTS REGARDING YOUR COMPLAINTS THAT ALLEGES FALSE NEGATIVE OR DISCREPANT RESULTS WHEN USING KIT BD VERITOR FOR RAPID DETECTION OF SARS-COV-2 (MN# (B)(4). ), BATCH NUMBER UNKNOWN. BD QUALITY PERFORMS A SYSTEMATIC APPROACH TO INVESTIGATE FALSE NEGATIVE COMPLAINTS. THIS APPROACH INVOLVES REVIEW OF MANUFACTURING BATCH HISTORY RECORDS, TESTING OF RETENTION SAMPLES, AND TESTING OF CUSTOMER RETURNED SAMPLES IF APPLICABLE. THE INVESTIGATION COULD NOT BE PERFORMED AS NO BATCH NUMBER WAS PROVIDED. THE COMPLAINT WAS UNABLE TO BE CONFIRMED. BD QUALITY WILL CONTINUE TO MONITOR FOR TRENDS. THERE WERE NO CORRECTIVE ACTIONS TAKEN AT THIS TIME.

    Description of Event or Problem · 0

    IT WAS REPORTED WHILE TESTING FOR SARS COV-2 POTENTIAL FALSE NEGATIVE RESULTS WERE OBTAINED. THERE WAS NO FORM OF REPEAT OR CONFIRMATORY TESTING REPORTED BY THE CUSTOMER. BD HAS ATTEMPTED TO CONTACT THE CUSTOMER MULTIPLE TIMES FOR ADDITIONAL INFORMATION REGARDING THIS EVENT WITH NO RESPONSE FROM THE CUSTOMER AT THIS TIME. THERE WAS NO INDICATION THAT RESULTS WERE REPORTED OUR OR ANY REPORT OF PATIENT IMPACT. (B)(4)

    Additional Manufacturer Narrative · 1

    MEDICAL DEVICE EXPIRATION DATE: UNKNOWN. A DEVICE EVALUATION IS ANTICIPATED BUT HAS NOT YET BEGUN. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED. DEVICE MANUFACTURE DATE: UNKNOWN. (B)(4).

    Description of Event or Problem · 1

    IT WAS REPORTED WHILE TESTING FOR SARS COV-2 POTENTIAL FALSE NEGATIVE RESULTS WERE OBTAINED. THERE WAS NO FORM OF REPEAT OR CONFIRMATORY TESTING REPORTED BY THE CUSTOMER. BD HAS ATTEMPTED TO CONTACT THE CUSTOMER MULTIPLE TIMES FOR ADDITIONAL INFORMATION REGARDING THIS EVENT WITH NO RESPONSE FROM THE CUSTOMER AT THIS TIME. THERE WAS NO INDICATION THAT RESULTS WERE REPORTED OUR OR ANY REPORT OF PATIENT IMPACT. (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1269474 BD RAPID DETECTION OF SARS-COV-2 VERITOR CORONAVIRUS ANTIGEN DETECTION SYSTEM QKP BECTON, DICKINSON & CO. (SPARKS) UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1