BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ENTERALITE INFINITY ENTERAL FEEDING PUMP

    MDR report key: 21377346 · Received February 13, 2025

    Report

    Report Number
    1722139-2025-00069
    Event Type
    Malfunction
    Date Received
    February 13, 2025
    Date of Event
    January 15, 2025
    Report Date
    January 15, 2025
    Manufacturer
    MOOG MEDICAL DEVICES GROUP
    Product Code
    LZH
    UDI-DI
    10814844000075
    PMA / PMN Number
    K031199
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    BIOMEDICAL ENGINEER
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    THE DEVICE WAS NOT RETURNED TO MMD FOR EVALUATION. A DHR REVIEW WAS COMPLETED AND NO NON-CONFORMANCES WERE FOUND. BECAUSE THE DEVICE WAS NOT RETURNED TO MMD FOR EVALUATION, AN INVESTIGATION COULD NOT BE COMPLETED. THIS REPORT WILL BE UPDATED IF THE DEVICE IS RETURNED TO MMDG.

    Additional Manufacturer Narrative · 0

    THE DEVICE WAS RETURNED TO MMD FOR EVALUATION. A DHR REVIEW WAS COMPLETED AND NO NON-CONFORMANCES WERE FOUND. WHEN THE DEVICE WAS RETURNED TO MMD FOR INVESTIGATION, IT DID OVER INFUSE, HOWEVER, IT WAS STILL WITHIN THE VOLUMETRIC RANGE THAT MMD WOULD CONSIDER NOT REPORTABLE. BASED ON THIS INFORMATION, NO MDR WOULD HAVE BEEN REQUIRED.

    Description of Event or Problem · 0

    THE INITIAL REPORTER STATED THAT THE PUMP UNDER INFUSED AT A RATE THE MMD WOULD CONSIDER REPORTABLE. MMD DID FOLLOW UP WITH THE INITIAL REPORTER, WHO STATED THAT THE PATIENT HAD NOT EXPERIENCED ANY ADVERSE EFFECTS DUE TO THE COMPLAINT. NO ADDITIONAL INFORMATION WAS PROVIDED. (B)(4)

    Description of Event or Problem · 0

    THE INITIAL REPORTER STATED THAT THE PUMP UNDER INFUSED AT A RATE THE MMD WOULD CONSIDER REPORTABLE. MMD DID FOLLOW UP WITH THE INITIAL REPORTER, WHO STATED THAT THE PATIENT HAD NOT EXPERIENCED ANY ADVERSE EFFECTS DUE TO THE COMPLAINT. NO ADDITIONAL INFORMATION WAS PROVIDED. [COMPLAINT- (B)(4)].

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    100739 ENTERALITE INFINITY ENTERAL FEEDING PUMP ENTERAL INFUSION PUMP LZH MOOG MEDICAL DEVICES GROUP INFKIT2 N/A 10814844000075

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Prefer Not To Disclose