Events

Retiro De Equipo (Recall) de Device Recall Stryker Orthopaedics Restoration Gap Plate Screw

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 Stryker Howmedica Osteonics Corp..

¿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
    52713
  • Clase de Riesgo del Evento
    Class 3
  • Número del evento
    Z-2139-2009
  • Fecha de inicio del evento
    2009-06-26
  • Fecha de publicación del evento
    2009-09-14
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2010-07-27
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=83764
  • 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
    Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate - Product Code MEH
  • Causa
    Raw material supplied by a third party used to manufacture various medical devices does not comply with metallurgical requirements outlines in astm standard for titanium surgical implants.
  • Acción
    Stryker Orthopaedics issued "Urgent Product Recall" letters via Federal Express priority overnight beginning June 26, 2009 to Branches, Hospital Risk Management and Chief of Orthopaedics and Surgeons. All users are requested to examine their inventory, retrieve all affected product and return for reconciliation to Stryker Orthopaedics. Users are also requested to complete the enclosed Product Accountability Form and fax with necessary information to the firm at 1-201-831-6069. For further information, contact Stryker Orthopaedics at 1-201-831-5970.

Device

Device Recall Stryker Orthopaedics Restoration Gap Plate Screw
  • Modelo / Serial
    Catalog number: 2080-0040; GAP PLATE SCREWS PTDMKE 27-Jun-2013 GAP PLATE SCREWS T0MMKE 01-Jul-2013 GAP PLATE SCREWS PT9MKE 02-Jul-2013 GAP PLATE SCREWS 34HMLE 09-Jul-2013 GAP PLATE SCREWS 34EMLE 14-Jul-2013 GAP PLATE SCREWS JKRMLE 23-Jul-2013 GAP PLATE SCREWS JKPMLE 23-Jul-2013 GAP PLATE SCREWS NL3MME 27-Aug-2013 GAP PLATE SCREWS NL6MME 27-Aug-2013 GAP PLATE SCREWS NL5MME 27-Aug-2013 GAP PLATE SCREWS NL4MME 28-Aug-2013 GAP PLATE SCREWS 7E4MNE 17-Sep-2013 GAP PLATE SCREWS 7E5MNE 17-Sep-2013 GAP PLATE SCREWS MERN50 05-Dec-2013 GAP PLATE SCREWS MERN4Y 05-Dec-2013 GAP PLATE SCREWS MET81P 18-Dec-2013 GAP PLATE SCREWS MET81T 18-Dec-2013 GAP PLATE SCREWS MET81V 18-Dec-2013 GAP PLATE SCREWS MET81R 22-Dec-2013 GAP PLATE SCREWS MET969 30-Dec-2013 GAP PLATE SCREWS MET967 30-Dec-2013 GAP PLATE SCREWS MET9H3 30-Dec-2013 GAP PLATE SCREWS MHA5LL 18-Jan-2014 GAP PLATE SCREWS MHA5LM 18-Jan-2014 GAP PLATE SCREWS MHA5LN 18-Jan-2014 GAP PLATE SCREWS MHA5LK 18-Jan-2014 GAP PLATE SCREWS MHA779 18-Jan-2014
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    Worldwide Distribution
  • Descripción del producto
    Stryker Orthopaedics Restoration Gap Plate Screw; || Dia. 6.5 mm, Lnth 40 mm; || Made in USA, Sterile; || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430
  • Manufacturer
    Stryker Howmedica Osteonics Corp.

Manufacturer

Stryker Howmedica Osteonics Corp.
  • Dirección del fabricante
    Stryker Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah NJ 07430
  • Empresa matriz del fabricante (2017)
    Stryker
  • Source
    USFDA