BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ID NOW COVID 19 ASSAY

    MDR report key: 12485149 · Received September 16, 2021

    Report

    Report Number
    1221359-2021-02688
    Event Type
    Malfunction
    Date Received
    September 16, 2021
    Date of Event
    July 27, 2021
    Report Date
    December 2, 2021
    Manufacturer
    ABBOTT DIAGNOSTICS SCARBOROUGH, INC.
    Product Code
    QJR
    UDI-DI
    10811877011320
    PMA / PMN Number
    EUA2000074
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ID
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    ADDITIONAL DATA: H10: TESTING WAS PERFORMED AT ABBOTT DIAGNOSTICS SCARBOROUGH, INC. ON RETAINED KIT LOT M159271 WITH INTERNAL POSITIVE QUALITY CONTROL SAMPLES AND NEGATIVE QUALITY CONTROL SWABS. ALL TEST RESULTS WERE VALID AND PERFORMED AS EXPECTED. ADDITIONALLY, THE MANUFACTURING RECORDS AND QUALITY CONTROL RELEASE TESTING WAS REVIEWED FOR TEST KIT PART NUMBER 191-000 / LOT: M159271 , TEST BASE PART NUMBER 190-430/ LOT: M159271 THE LOT MET THE REQUIRED RELEASE SPECIFICATIONS. A REVIEW OF THE COMPLAINTS REPORTED AS FALSE POSITIVE (CONFIRMED AND UNCONFIRMED, CONFLICTING RESULTS) RELATED TO KIT LOT M159271 SHOWED THAT THE COMPLAINT RATE IS (B)(4). IN CONCLUSION, ABBOTT DIAGNOSTICS SCARBOROUGH WAS UNABLE TO DETERMINE THE EXACT ROOT CAUSE OF THE REPORTED ISSUE AS THE LOGFILES WERE NOT PROVIDED . HOWEVER A POSSIBLE ASSIGNABLE ROOT CAUSE IS SAMPLE INTERFERENCE OR CROSS CONTAMINATION. MFR REFERENCE REPORTS: 1221359-2021-02667, 1221359-2021-02685, 1221359-2021-02686, 1221359-2021-02687, 1221359-2021-02689, 1221359-2021-02690, AND 1221359-2021-02691.

    Additional Manufacturer Narrative · 0

    THE INVESTIGATION IS STILL IN PROGRESS. A SUPPLEMENTAL REPORT WILL BE PROVIDED AFTER COMPLETION. MFR REFERENCE REPORTS: 1221359-2021-02667, 1221359-2021-02685, 1221359-2021-02686, 1221359-2021-02687, 1221359-2021-02689, 1221359-2021-02690, 1221359-2021-02691.

    Description of Event or Problem · 0

    THE CUSTOMER REPORTED ELEVEN (11) FALSE NEGATIVE RESULTS WITH THE ID NOW COVID-19 ASSAY FOR ELEVEN (11) PATIENTS PERFORMED ON BETWEEN 17JUL2021 TO 19AUG2021. THIS MFR. REPORT ADDRESSES PATIENT SEVEN (7) OF ELEVEN (11). THE CUSTOMER REPORTED A FALSE NEGATIVE RESULT WITH THE ID NOW COVID-19 ASSAY PERFORMED ON (B)(6) 2021 ON A DIRECT TESTED NASOPHARYNGEAL SWAB. REPEAT TESTING WAS NOT PERFORMED .ON THE SAME DAY PCR CONFIRMATION TESTING GENERATED A POSITIVE RESULT. NO ADDITIONAL PATIENT INFORMATION, INCLUDING TREATMENT AND OUTCOME, WAS PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1381458 ID NOW COVID 19 ASSAY MOLECULAR IVD FOR ID NOW COVID-19 QJR ABBOTT DIAGNOSTICS SCARBOROUGH, INC. M159271 10811877011320

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown