Retiro De Equipo (Recall) de Device Recall Custom Straight Accolade Common Name: Handle Classification Name: Orthopedics Manual Surgical Instr

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
    60744
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0804-2012
  • Fecha de inicio del evento
    2011-08-19
  • Fecha de publicación del evento
    2012-01-18
  • Estado del evento
    Terminated
  • País del evento
  • Fecha de finalización del evento
    2017-07-11
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
  • 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
    Orthopedic manual surgical instrument - Product Code LXH
  • Causa
    Stryker orthopaedics has become ware that there is the potential for the above referenced instruments to fracture in two pieces along the width of the body under the striking plate.
  • Acción
    Stryker Orthopaedics sent a Urgent Product Recall update dated August 18, 2011, via FedEx to all affected customers. The letter identified the product(s) the problem and the action needed to be taken by the customer. Our records indicate that you have received the above referenced product(s). It is Stryker's¿ responsibility as the manufacturer to ensure that customers who may have received these affected products also receive this important communication. Please assist us in meeting our regulatory obligation by faxing back the attached Product Recall Acknowledgment Form within 5 days to 201-831-6069. Please also contact the hospitals in your territory that have the affected product to arrange return of the product as replacement product becomes available. If you have any further questions please call (201) 831-5158.

Device

  • Modelo / Serial
    510 K exempt. All lots I-H08641400 CUSTOM STRAIGHT ACCOLADE  I-H08641400 CUSTOM STRAIGHT ACCOLADE  I-H08641400 CUSTOM STRAIGHT ACCOLADE  I-H08641400 CUSTOM STRAIGHT ACCOLADE  I-H1427HFOO "
  • Clasificación del producto
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    USA (nationwide distribution)
  • Descripción del producto
    Brand Name: Custom Straight Accolade¿¿ Common Name: Handle Classification Name: Orthopedics Manual Surgical Instrument || Brand Name: Specialty Straight Command¿¿ Common Name: Handle Classification Name: Orthopedics Manual Surgical Instrument || Brand Name: Custom Straight Accolade¿¿ || Common Name: Handle || Classification Name: Orthopedics Manual Surgical Instrument || Brand Name: Custom Accolade¿¿ Broach Handle || Common Name: Handle || Classification Name: Orthopedics Manual Surgical Instrument || Brand Name: Custom Accolade¿¿ Broach Handle || Common Name: Handle || Classification Name: Orthopedics Manual Surgical Instrument || Brand Name: Specialty Locking Accolade¿¿ Straight Broach Handle Common Name: Handle Classification Name: Orthopedics Manual Surgical Instrument || Brand Name: Specialty Woodpecker Adapted Accolade¿¿ Broach || Handle || Common Name: Handle || Classification Name: Orthopedics Manual Surgical Instrument || Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07430 || The Handles are instruments that attach to the femoral rasps or broaches to prepare the Femoral Canal in total hip replacement procedures. The rasps have a geometry similar to the final size and shape of the implant. The straight design allows the rasp handle to be used in standard or minimally invasive approaches because it minimizes the contact with adjacent soft tissue. The Handle is impacted with a slotted mallet on the top and on the bottom portions of the striking plate, to achieve rasp insertion and extraction respectively. The handles share the same geometry in the region that is of interest in this matter.
  • Manufacturer

Manufacturer

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