BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BINAXNOW COVID-19 AG SELF TEST 2CT

    MDR report key: 18434795 · Received January 3, 2024

    Report

    Report Number
    1221359-2024-00014
    Event Type
    Malfunction
    Date Received
    January 3, 2024
    Date of Event
    December 18, 2023
    Report Date
    March 18, 2024
    Manufacturer
    ABBOTT DIAGNOSTICS SCARBOROUGH, INC.
    Product Code
    QKP
    UDI-DI
    00811877011408
    PMA / PMN Number
    EUA210264
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 0

    FDA UDI-(B)(6) TESTING WAS PERFORMED AT ABBOTT DIAGNOSTICS SCARBOROUGH, INC. ON RETAINED KIT LOT 203487 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 195-160/ LOT 203487 AND TEST BASE PART NUMBER 195-430H/ LOT 197871. THE LOT MET THE REQUIRED RELEASE SPECIFICATIONS. A REVIEW OF THE COMPLAINTS REPORTED FALSE NEGATIVE PATIENT RESULTS (CONFIRMED AND UNCONFIRMED, CONFLICTING RESULTS) RELATED TO KIT LOT 203487 SHOWED THAT THE COMPLAINT RATE IS (B)(4). ABBOTT DIAGNOSTICS SCARBOROUGH WAS UNABLE TO DETERMINE THE EXACT ROOT CAUSE OF THE REPORTED ISSUE, HOWEVER IT COULD HAVE POSSIBLY BEEN RELATED TO ISSUES INCLUDING THE SELF-TEST USER PERFORMANCE, INTERPRETATION OF THE RESULT, OR THE SPECIFIC PATIENT SAMPLE. H3 OTHER TEXT : SINGLE USE; DEVICE DISCARDED.

    Additional Manufacturer Narrative · 0

    FDA UDI-(B)(4). THE REMAINDER OF THE INVESTIGATION REMAINS IN PROGRESS. A SUPPLEMENTAL REPORT WILL BE PROVIDED AFTER COMPLETION. H3 OTHER TEXT : SINGLE USE; DEVICE DISCARDED.

    Description of Event or Problem · 0

    THE CONSUMER REPORTED EIGHT (8) FALSE NEGATIVE RESULTS WITH THE BINAXNOW COVID-19 ANTIGEN SELF-TEST WITH THREE (3) LOTS PERFORMED ON (B)(6)2023. THIS MANUFACTURER'S REPORT ADDRESSES TEST ONE (5) OF EIGHT (8) AND LOT 203487 (TOTAL QUANTITY: 2). CONFIRMATION TESTING WAS NOT PERFORMED. REPEAT TESTING WAS PERFORMED SEVEN TIMES ON THE SAME DAY, EACH GENERATING NEGATIVE RESULTS. THE CONSUMER PERFORMED PRIOR TESTING USING AN UNKNOWN BRAND OF ANTIGEN SELF-TEST ON 11DEC2023 THAT GENERATED A POSITIVE RESULT. THE CONSUMER WAS CONTINUING TO EXPERIENCE SYMPTOMS LIKE STUFFY NOSE, COUGH, AND A CONSTANT RUNNY NOSE. NO ADDITIONAL PATIENT INFORMATION, INCLUDING TREATMENT AND OUTCOME, WAS PROVIDED.

    Description of Event or Problem · 0

    THE CONSUMER REPORTED EIGHT (8) FALSE NEGATIVE RESULTS WITH THE BINAXNOW COVID-19 ANTIGEN SELF-TEST WITH THREE (3) LOTS PERFORMED ON (B)(6)2023. THIS MANUFACTURER'S REPORT ADDRESSES TEST ONE (5) OF EIGHT (8) AND LOT 203487 (TOTAL QUANTITY: (B)(4). CONFIRMATION TESTING WAS NOT PERFORMED. REPEAT TESTING WAS PERFORMED SEVEN TIMES ON THE SAME DAY, EACH GENERATING NEGATIVE RESULTS. THE CONSUMER PERFORMED PRIOR TESTING USING AN UNKNOWN BRAND OF ANTIGEN SELF-TEST ON (B)(6)2023 THAT GENERATED A POSITIVE RESULT. THE CONSUMER WAS CONTINUING TO EXPERIENCE SYMPTOMS LIKE STUFFY NOSE, COUGH, AND A CONSTANT RUNNY NOSE. NO ADDITIONAL PATIENT INFORMATION, INCLUDING TREATMENT AND OUTCOME, WAS PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1507597 BINAXNOW COVID-19 AG SELF TEST 2CT CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM. QKP ABBOTT DIAGNOSTICS SCARBOROUGH, INC. 203487 00811877011408

    Patients

    Seq Age Sex Outcome Treatment
    1 43 YR Female