BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ALINITY I SYPHILIS TP REAGENT KIT

    MDR report key: 25209494 · Received May 18, 2026

    Report

    Report Number
    3002809144-2026-00128
    Event Type
    Malfunction
    Date Received
    May 18, 2026
    Date of Event
    May 11, 2026
    Report Date
    May 18, 2026
    Manufacturer
    ABBOTT GMBH
    Product Code
    LIP
    UDI-DI
    00380740162009
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CH
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    COMPLETE ENTRY FOR SECTION A1 - PATIENT IDENTIFIER: (B)(6). AN EVALUATION IS IN PROCESS. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE EVALUATION IS COMPLETE. SECTION A PATIENT INFORMATION: REFER TO SECTION B5 FOR COMPLETE PATIENT INFORMATION. THIS REPORT IS BEING FILED ON AN INTERNATIONAL PRODUCT, LIST NUMBER 07P60-77 THAT HAS A SIMILAR PRODUCT DISTRIBUTED IN THE US, LIST NUMBER 7P60-21 / 31, WITH 510K NUMBER K153730.

    Description of Event or Problem · 0

    THE CUSTOMER OBSERVED FALSE NEGATIVE ALINITY I SYPHILIS RESULTS GENERATED ON AN ALINITY I PROCESSING MODULE FOR TWO ELDERLY MALE PATIENTS. THE FOLLOWING DATA WAS PROVIDED: SID (B)(6) (62-YEAR-OLD MALE) ALINITY I SYPHILIS = 0.89, JOHNSON & JOHNSON = 1.3, ROCHE = 1.03, TPPA = SUSPICIOUS, RPR = NEGATIVE. SID (B)(6) (72-YEAR-OLD MALE) ALINITY I SYPHILIS = 0.93, JOHNSON& JOHNSON = 3.4, TPPA WEAK POSITIVE, RPR = NEGATIVE THERE WAS NO IMPACT TO PATIENT MANAGEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    331965 ALINITY I SYPHILIS TP REAGENT KIT ENZYME LINKED IMMUNOABSORPTION ASSAY, TREPONEMA PALLIDUM LIP ABBOTT GMBH 81332BE01 00380740162009

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown ALNTY I PR MOD CN, 03R65-20, (B)(6).