BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    8100 ALARIS PUMP MODULE

    MDR report key: 11043417 · Received December 20, 2020

    Report

    Report Number
    2016493-2020-74133
    Event Type
    Malfunction
    Date Received
    December 20, 2020
    Report Date
    March 7, 2018
    Manufacturer
    CAREFUSION SD
    Product Code
    FRN
    UDI-DI
    10885403810015
    PMA / PMN Number
    K133532
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 1

    THE CUSTOMER REPORTED PROBLEM WAS CONFIRMED. THE DEVICE WAS REPAIRED, RETESTED, AND RETURNED TO THE CUSTOMER. A REVIEW OF THE DEVICE HISTORY RECORD IN SAP FOR SN (B)(4) WAS PERFORMED FROM THE DATE OF THE MANUFACTURE TO DATE OF THE RELEASE OF PRODUCT, WHICH CONFIRMED THAT THIS DEVICE WAS NOT INVOLVED IN A PRODUCTION FAILURE, AND PRODUCT WAS RETURNED FOR SERVICING WHICH CORRELATES TO THE CUSTOMER REPORTED ISSUE. A REVIEW OF THE COMPLAINT HISTORY RECORD IN THE TRACKWISE WAS PERFORMED FOR THE SN (B)(4) WHICH CONFIRMED NO SIMILAR COMPLAINTS WITH THE SAME OR RELATED FAILURE MODE. THE CUSTOMER STATED THAT THERE WAS NO PATIENT INVOLVEMENT.

    Description of Event or Problem · 1

    LVP BEZEL POST RECALL 2017- 03/07/2018 11:49:57 JEANNETTE KENEFICK (JKENEFIC) CONTACT: GREG BARBER - BIOMED TECH 410-787-4469 [email protected] 03/20/2018 13:00:20 TAM S LUONG (TLUONG) BEZEL NOT AFFECTED RECALL. EST MAJOR 04/12/2018 12:40:05 JESSICA GALANG (JGALANG) UPDATED FROM RCL TO MJR FOR THE MAJOR REPAIR NEEDED PER TAM LUONG, SERVICE TECH. REPAIR APPROVED BY GREG BARBER AT FOR $365. NEW PO# IS S1899892SM. NPI 04/17/2018 06:50:20 TAM S LUONG (TLUONG) VERIFIED BEZEL NOT AFFECTED RECALL. REPLACED BEZEL FOR CRACKED. REPLACED NON ALARIS FRONT CASE KEYPAD, DOOR COVER, DOOR LATCH. REPLACED REAR CASE FOR CRACKED. REPLACED IUI FOR CORRODED. TESTED RUN-IN OK 04/17/2018 07:04:46 TAM S LUONG (TLUONG) RETURN NON ALARIS PARTS TO CUST FOR REQUEST 04/17/2018 10:45:14 ANNETTE A MENDEZ (AMENDEZ) 1Z9791540272269041 07/31/2019 09:10:32 JOSEPH KUHLS (JKUHLS) DURING THE REPAIR PROCESS, IT WAS DETERMINED THAT THE ORIGINAL PROBLEM CODE SHOULD HAVE BEEN BROK (BROKEN DAMAGED) FOR COMPLAINT TRENDING PURPOSES FILE REOPENED TO ADD TRACK WISE PR NUMBER TO THE DEVICE DATA FIELD. THIS FILE WAS INITIALLY CLASSIFIED AS A LEVEL 3 NON-COMPLAINT FOR PREVENTATIVE MAINTENANCE, UPGRADE, RECONDITIONING, CUSTOMER INQUIRY, OR RECALL WHICH DO NOT REQUIRE CUSTOMER ADVOCACY QUALITY REVIEW, PER SWI 1501-006-000. THIS FILE CONTAINED DOCUMENTATION OF PRODUCT DEFICIENCY ALLEGATIONS, PER SWI-151-070-000 AND SWI 1501-096-000, AND/OR REPAIRS (WHICH MAY OR MAY NOT HAVE BEEN PERFORMED) THAT ARE OUT-OF-SCOPE WITH THE INITIAL LEVEL 3 NON-COMPLAINT. SUCH DOCUMENTATION UPGRADED THE FILE TO A LEVEL 2 COMPLAINT, PER SWI 1501-070-000 AND SWI-096-000, WHICH REQUIRED A LEVEL 2 CUSTOMER ADVOCACY QUALITY REVIEW, ALSO PER SWI 1501-070-000.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1508402 8100 ALARIS PUMP MODULE PUMP, INFUSION FRN CAREFUSION SD 8100 10885403810015

    Patients

    Seq Age Sex Outcome Treatment
    1