BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ID NOW COVID-19 2.0 TEST KIT 24T (EUA)

    MDR report key: 16315160 · Received February 7, 2023

    Report

    Report Number
    1221359-2023-00235
    Event Type
    Malfunction
    Date Received
    February 7, 2023
    Date of Event
    January 26, 2023
    Report Date
    April 28, 2023
    Manufacturer
    ABBOTT DIAGNOSTICS SCARBOROUGH, INC.
    Product Code
    QJR
    UDI-DI
    00811877011354
    PMA / PMN Number
    EUA210517
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    THE REMAINDER OF THE INVESTIGATION REMAINS IN PROGRESS. A SUPPLEMENTAL REPORT WILL BE PROVIDED AFTER COMPLETION. DEVICE EVALUATED BY MFR: SINGLE USE DEVICE, DISCARDED.

    Additional Manufacturer Narrative · 0

    TESTING WAS PERFORMED AT ABBOTT DIAGNOSTICS SCARBOROUGH, INC. ON RETAINED KIT LOT 1100027 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 KIT PART NUMBER 192-000 / LOT 1100027 AND TEST BASE PART NUMBER 192-430 / LOT 1100027. THE LOT MET THE REQUIRED RELEASE SPECIFICATIONS. A REVIEW OF THE COMPLAINTS REPORTED AS FALSE POSITIVE PATIENT RESULTS (CONFIRMED AND UNCONFIRMED, CONFLICTING RESULTS) RELATED TO KIT LOT 1100027 SHOWED THAT THE COMPLAINT RATE IS (B)(4)%. 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 PATIENT SAMPLE INTERFERENCE. H3 OTHER TEXT : SINGLE USE DEVICE, DISCARDED.

    Description of Event or Problem · 0

    CUSTOMER REPORTED TWO (2) FALSE POSITIVE RESULTS WITH ID NOW COVID-19 2.0 ASSAY FOR MULTIPLE LOTS, TAKEN ON (B)(6) 2023. THIS MFR. REPORT ADDRESSES TEST TWO (2) OF TWO (2), LOT 1100027. CONFIRMATION TESTING WAS COMPLETED ON THE SAME DAY, (B)(6) 2023, USING A NASAL PHARYNGEAL SAMPLE IN VTM WAS AND SENT TO DIASORIN, GENERATING A NEGATIVE TEST RESULT. NO ADDITIONAL PATIENT INFORMATION, INCLUDING TREATMENT AND OUTCOME, WAS PROVIDED.

    Description of Event or Problem · 0

    THE CUSTOMER REPORTED TWO (2) FALSE POSITIVE RESULTS WITH ID NOW COVID-19 2.0 ASSAY FOR MULTIPLE LOTS, TAKEN ON (B)(6) 2023. THIS MFR. REPORT ADDRESSES TEST TWO (2) OF TWO (2), LOT 1100027. CONFIRMATION TESTING WAS COMPLETED ON THE SAME DAY, (B)(6) 2023, USING A NASAL PHARYNGEAL SAMPLE IN VTM WAS AND SENT TO DIASORIN, GENERATING A NEGATIVE TEST RESULT. NO ADDITIONAL PATIENT INFORMATION, INCLUDING TREATMENT AND OUTCOME, WAS PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    927690 ID NOW COVID-19 2.0 TEST KIT 24T (EUA) REAGENTS, 2019-NOVEL CORONAVIRUS NUCLEIC ACID QJR ABBOTT DIAGNOSTICS SCARBOROUGH, INC. 1100027 00811877011354

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown