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  • Dispositivo 374
  • Fabricante 58
  • Evento 124969
  • Implante 1
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0403-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30875
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0404-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30876
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0405-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30877
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0406-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30878
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0407-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30879
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0408-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30880
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0409-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30881
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0410-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30882
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0411-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30883
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0412-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30884
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0413-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30885
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0414-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30886
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0415-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30887
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0416-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30888
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0417-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30889
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall Access Cardiosystems
  • Tipo de evento
    Recall
  • ID del evento
    27992
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0356-04
  • Fecha de inicio del evento
    2003-12-19
  • Fecha de publicación del evento
    2004-07-20
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-07-13
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30890
  • 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
    Automated External Defibrillators (Non-Wearable) - Product Code MKJ
  • Causa
    Difibrillator may fail to operate due to a faulty component on the circuit board.
  • Acción
    Access CardioSystems notified Distributors by telephone and email on 12/18/03 and 12/19/03. Recall letters were dated 12/19/03 and issued by US Mail. Distributors are requested to locate and return AED's .
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0418-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30891
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0419-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30893
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0420-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30894
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0421-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30895
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0422-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30896
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0423-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30897
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0424-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30899
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0425-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30900
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
Retiro De Equipo (Recall) de Device Recall ACE trochanteric nail systems
  • Tipo de evento
    Recall
  • ID del evento
    27923
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0426-04
  • Fecha de inicio del evento
    2003-12-11
  • Fecha de publicación del evento
    2004-01-31
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-04-15
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30901
  • 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
    Rod, Fixation, Intramedullary And Accessories - Product Code HSB
  • Causa
    The lag screw may migrate to the femoral head or into the abdominal cavity.
  • Acción
    Recall letters dated 12/15/03 were issued to receiving hospitals. Hospitals were instructed to cease implantation, quarantine stocks, and to notify implanting physicians to monitor their patients.
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Aviso

Los dispositivos médicos ayudan con el diagnóstico, la prevención y el tratamiento de muchas lesiones y enfermedades. A través de la International Medical Devices Database no estamos sugiriendo que compañías u otras entidades mencionadas en la base de datos hayan sido parte de una conducta ilegal o hayan actuado de manera impropia. Un mismo dispositivo médico puede tener distintos nombres en diferentes países. Esta base de datos no busca proporcionar asesoría médica. Los pacientes deben consultar con sus médicos para determinar si la data contiene información relevante y si la misma tiene implicaciones médicas para ellos.