Events

Retiro De Equipo (Recall) de Sigma Spectrum Infusion Pump with master Drug Library Version 6.

Según U.S. Food and Drug Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en United States que fue producido por Baxter Healthcare Corporation.

¿Qué es esto?

Una corrección al equipo o acción de retiro tomada por el fabricante para abordar un problema con un dispositivo médico. Los retiros (recalls) ocurren cuando un dispositivo médico está defectuoso, cuando puede poner en riesgo la salud, o cuando simultáneamente está defectuoso y puede poner en riesgo la salud.

Más información acerca de la data acá
  • Tipo de evento
    Recall
  • ID del evento
    79815
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-1664-2018
  • Fecha de inicio del evento
    2018-04-03
  • Fecha de publicación del evento
    2018-05-04
  • Estado del evento
    Open, Classified
  • País del evento
    United States
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=163555
  • Notas / Alertas
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Notas adicionales en la data
    Pump, infusion - Product Code FRN
  • Causa
    Service technician improperly documented final release testing on product, indicating that the full battery of release tests were performed when, in fact, several tests were omitted. he omitted tests include air-in-line detection at 400ml/hr and 800ml/hr and verification of upstream occlusion detection at 800ml/hr. improper detection of air-in-line or upstream occlusion may result in serious adverse health consequences.
  • Acción
    On 4/3/18, Baxter HealthCare Corporation mailed URGENT MEDICAL DEVICE CORRECTION notices and Reply Forms to customers via first class mail. Actions to be Taken by Customers: 1. Locate and discontinue use of all affected pumps at your facility. 2. Return the device to Baxter for testing. To arrange for return of affected devices, contact Baxter at 800-356-3454 between the hours of 7:00 am and 7:00 pm Eastern Time, Monday through Friday. Please have your Baxter 8-digit ship-to account number, product code, serial number, and quantity of devices to be returned ready when calling. 3. If you purchased this product directly from Baxter, complete the enclosed Baxter Customer Reply Form and return it to Baxter by faxing it to 224-270-5457 or via email to fca@baxter.com even if you do not have inventory. 4. If you purchased this product from a distributor, please note that the Baxter customer reply form is not applicable. If a reply form is provided by your distributor or wholesaler, please return it to the supplier according to their instructions. 5. If you distribute this product to other facilities or departments within your institution, please forward a copy of this communication to them. 6. If you are a dealer, wholesaler, distributor/reseller, or original equipment manufacturer (OEM) that distributed any affected product to other facilities, please notify your customers.

Device

Sigma Spectrum Infusion Pump with master Drug Library Version 6.
  • Modelo / Serial
    Serial Numbers 709860 735355 743891 749663 753665 757109 763909 768077 774906 776397 780931 785500 789177 791625 792667 794258 797835 798697 799183 801072 802788 803224 804175 804202 804235 804561 804988 806824 811741 812442 812989 813180 844637 844720 845844 846093 846115 858309 864606 864957 870921 872713 872941 873294 873296 873302 877416 879360 883764 885021 905402 910300 912661 914647 915558 921852 923011 923362 923483 923990 926408 926680 927374 927490 927810 927848 928705 929190 929572 929887 930694 930914 930972 931613 931745 932170 932315 932496 932601 933050 933625 933745 934174 934407 934629 934656 934684 934685 935474 935554 935636 936378 936422 937342 938176 938742 939342 939364 939571 942194 945100 962029 965017 965310 967527 982596 983087 996433 996840 997035 997317 999136 1000594 1006058 1006935 1008672 1011288 1011482 1012217 1012228 1012708 1012883 1013017 1013180 1013371 1013628 1015173 1015537 1015796 1015902 1016229 1016277 1016287 1017064 1017616 1017627
  • Clasificación del producto
    General Hospital and Personal Use Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    US Nationwide & Puerto Rico
  • Descripción del producto
    Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version 6) 35700BAXL || Product Usage: || The Baxter Sigma Spectrum Infusion Pump with master Drug Library is intended to be used for the controlled administration of fluids. These fluids may includes pharmaceutical drugs, blood, blood products and mixture if required patient therapy. The intended routes of administration consist of the following clinically accepted routes: intravenous, arterial, subcutaneous, intrathecal, epidural or irrigation of fluids. Spectrum infusion pump is intended to be used in conjunction with legally marketed intravenous administration sets and medications provided by user. The Spectrum and Spectrum with MAster Drug Library is intended to reduce operator interaction through automated programming thereby helping to reduce errors associated with complex device programming.
  • Manufacturer
    Baxter Healthcare Corporation

Manufacturer

Baxter Healthcare Corporation
  • Dirección del fabricante
    Baxter Healthcare Corporation, 711 Park Ave, Medina NY 14103-1036
  • Empresa matriz del fabricante (2017)
    Baxter International
  • Source
    USFDA