BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRELLA BED

    MDR report key: 24991449 · Received April 25, 2026

    Report

    Report Number
    1824206-2026-00940
    Event Type
    Malfunction
    Date Received
    April 25, 2026
    Date of Event
    March 31, 2026
    Report Date
    April 25, 2026
    Manufacturer
    BAXTER HEALTHCARE CORPORATION
    Product Code
    FNL
    UDI-DI
    00887761985162
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    THE BAXTER TECHNICIAN FOUND THE BRAKE CASTERS NEEDED TO BE REPLACED. PER THE BAXTER SERVICE MANUAL, IT IS NECESSARY FOR THE CENTRELLA BED TO HAVE AN EFFECTIVE MAINTENANCE PROGRAM. WE RECOMMEND THAT YOU DO ANNUAL PREVENTIVE MAINTENANCE. CHECK THE BRAKES TO SEE WHETHER THE BED MOVES WHEN THE BRAKES ARE SET. REPLACE PARTS OR ADJUST THE SYSTEM IF NECESSARY. A SEARCH OF THE BAXTER MAINTENANCE RECORDS SHOWED BAXTER PERFORMED PREVENTIVE MAINTENANCE ON THIS BED ON AUG 218, 2025. IT IS UNKNOWN IF THE FACILITY PERFORMED ANY OTHER PREVENTIVE MAINTENANCE ON THIS BED. THE TECHNICIAN REPLACED THE BRAKE CASTERS TO RESOLVE THE REPORTED EVENT. BASED ON THIS INFORMATION, NO FURTHER ACTION IS REQUIRED.

    Description of Event or Problem · 0

    DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT CENTRELLA MED-SURG HAD BRAKES WERE NOT HOLDING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    600423 CENTRELLA BED BED, AC-POWERED ADJUSTABLE HOSPITAL FNL BAXTER HEALTHCARE CORPORATION P7900B 00887761985162

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown