BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ENTERALITE INFINITY ORANGE ENTERAL FEEDING PUMP

    MDR report key: 20970839 · Received December 18, 2024

    Report

    Report Number
    1722139-2024-00699
    Event Type
    Malfunction
    Date Received
    December 18, 2024
    Date of Event
    November 22, 2024
    Report Date
    November 22, 2024
    Manufacturer
    MOOG MEDICAL DEVICES GROUP
    Product Code
    LZH
    UDI-DI
    10814844000341
    PMA / PMN Number
    K031199
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    BIOMEDICAL ENGINEER
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    THE DEVICE WAS RETURNED TO MMD FOR EVALUATION. A DHR REVIEW WAS COMPLETED AND DID NOT SHOW THE CURRENTLY REPORTED ISSUE. WHEN THE DEVICE WAS RETURNED TO MMD FOR INVESTIGATION, IT OPERATED AS EXPECTED. MMD COULD NOT REPLICATE OR CONFIRM THE REPORTED COMPLAINT. BASED ON THIS INFORMATION, NO MDR WOULD HAVE BEEN REQUIRED.

    Additional Manufacturer Narrative · 0

    THE DEVICE WAS NOT RETURNED TO MMD FOR EVALUATION. A DHR REVIEW WAS COMPLETED AND DID NOT SHOW THE CURRENTLY REPORTED ISSUE. 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.

    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 COMPLAINT OCCURRED DURING TESTING AND HAD NOT HAD ANY EFFECT ON A PATIENT. NO ADDITIONAL INFORMATION WAS PROVIDED. [COMPLAINT-(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 COMPLAINT OCCURRED DURING TESTING AND HAD NOT HAD ANY EFFECT ON A PATIENT. NO ADDITIONAL INFORMATION WAS PROVIDED. (B)(4)].

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2083726 ENTERALITE INFINITY ORANGE ENTERAL FEEDING PUMP ENTERAL INFUSION PUMP LZH MOOG MEDICAL DEVICES GROUP INFORNGRF N/A 10814844000341

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown