BEUDAMED
    FDA Adverse Event Other Summary report: N

    IRRISEPT

    MDR report key: 18436757 · Received January 2, 2024

    Report

    Report Number
    MW5149728
    Event Type
    Other
    Date Received
    January 2, 2024
    Report Date
    December 28, 2023
    Manufacturer
    IRRIMAX CORPORATION
    Product Code
    FQH
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    NEAR MISS EVENT IN OUR PERIOPERATIVE SATELLITE. RN ASKING FOR "IRRISEPT" THAT IS A CHLORHEXIDINE MIXTURE THAT COMES FROM SUPPLY CHAIN AND NOT PHARMACY. PHARMACY STAFF HEARD "ARICEPT". THIS WAS RESOLVED WHEN THE PHARMACIST CALLED THE OPERATING ROOM FOR CLARIFICATION. ISMP, (B)(6).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1699618 IRRISEPT LAVAGE, JET FQH IRRIMAX CORPORATION

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown ARICEPT