Events

Retiro De Equipo (Recall) de Device Recall OsteoClage Stainless Steel Bone Plate

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 Acumed LLC.

¿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
    67885
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-1515-2014
  • Fecha de inicio del evento
    2014-03-26
  • Fecha de publicación del evento
    2014-04-25
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2015-02-04
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=126557
  • 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
    Pin, fixation, smooth - Product Code HTY
  • Causa
    Manufacturing of these devices with a grade of stainless steel that is not within specifications.
  • Acción
    Acumed sent an Urgent Medical Device Recall letter dated March 26, 2014 to all affected customers. The letter identified the affected products, problem and actions to be taken. Customers are instructed to immediately stop using and/or distributing all lots identified in the letter. Return affected products as instructed in the letter. For questions contact Acumed Business Service via email at BusinessService@acumed.net or via phone at 877-627-9957.

Device

Device Recall OsteoClage Stainless Steel Bone Plate
  • Modelo / Serial
    2.0mm x 80mm SS cable/sleeve: Lot # 222078, 232175, 245032, 254368, 261903, 270659, 284155, 297281.  2.0mm SS sleeve only: Lot # 247553, 267469, 280871, 313261.  8, 7 hole SS compression plate: Lot # 300381.  10, 9 hole SS compression plate: Lot # 299641.
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    US Nationwide Distribution - in the states of CA, CO, FL, GA, LA, MI, MN, MO, OH, OR, PA, PR, TX, UT, VA, WA and WY. Product was distributed outside the US to: Australia, China, Figi, France, Great Britain, Italy, Japan, Korea, Maylasia, Sweden, South Africa, Spain.
  • Descripción del producto
    The Osteo-Clage System consists of stainless steel cable/sleeves and compression plates. . || 2.0 mm x 850mm SS Cable/Sleeve; Part Number 01-0020-S || 2.0 mm SS Sleeve Only; Part Number 01-0022-S || 8, 7 hole, SS compression plate; Part Number 02-2007-S || 10, 9 hole, SS compression plate; Part Number 02-2009-S || Product Usage: The Osteo-Clage Stainless Steel Bone Plate is an implantable straight, rigid stainless steel plate. It is used in conjunction with 4.5mm Cortical bone screws to provide compression across bone fractures. The Osteo-Clage Cerclage Wire Crimp sleeve is used in conjunction with the bone plate in cerclage fixation procedures
  • Manufacturer
    Acumed LLC

Manufacturer

Acumed LLC
  • Dirección del fabricante
    Acumed LLC, 5885 NW Cornelius Pass Rd, Hillsboro OR 97124-9432
  • Empresa matriz del fabricante (2017)
    Acumed Llc
  • Source
    USFDA