BEUDAMED
    FDA Adverse Event Other Summary report: N

    CATHETER, INTRAVASCULAR, THERAPEUTIC, LONG-TERM GREATER THAN 30 DAYS

    MDR report key: 24710618 · Received March 30, 2026

    Report

    Report Number
    MW5186067
    Event Type
    Other
    Date Received
    March 30, 2026
    Date of Event
    March 24, 2026
    Report Date
    March 25, 2026
    Manufacturer
    TELEFLEX LLC (NADC)
    Product Code
    LJS
    Report Source
    Voluntary report
    Reporter Location
    US
    Reporter Occupation
    PHARMACIST
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    PT EXPERIENCED ANAPHYLAXIS AFTER PCC LINE PLACEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    770233 CATHETER, INTRAVASCULAR, THERAPEUTIC, LONG-TERM GREATER THAN 30 DAYS CATHETER, INTRAVASCULAR, THERAPEUTIC, LONG-TERM GREATER THAN 30 DAYS LJS TELEFLEX LLC (NADC) 33F25E0833

    Patients

    Seq Age Sex Outcome Treatment
    1 57 YR Male Other