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  • Dispositivo 26490
  • Fabricante 33665
  • Evento 35826
  • Implante 7175
Retiro De Equipo (Recall) de Central Venous Tray, Triple Lumen Polyurethane
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1178-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97237
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Central Venous Tray, Triple Lumen Polyurethane
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1177-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97236
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Central Venous Tray, Triple Lumen Polyurethane
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1176-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97235
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Central Venous Tray, Triple Lumen Polyurethane
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1175-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97234
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Tri...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1174-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97233
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Tri...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1173-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97232
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Fiv...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1172-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97231
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Trip...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1171-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97230
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Tri...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1170-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97229
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated 5 L...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1169-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97228
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated 5 L...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1168-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97227
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Dou...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1167-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97226
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Dou...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1166-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97225
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Dou...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1165-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97224
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Dou...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1164-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97223
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Dou...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1163-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97222
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Dou...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1162-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97221
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Dou...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1161-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97220
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Dou...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1160-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97219
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Dou...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1159-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97218
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Soft Central Venous Tray, Minocycline/Rifampin Impregnated...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1158-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97217
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Do...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1157-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97216
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Tr...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1156-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97215
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous CatheterTray, Minocycline/Rifampin Impregn...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1155-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97214
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
Retiro De Equipo (Recall) de Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Tr...
  • Tipo de evento
    Recall
  • ID del evento
    57663
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-1154-2011
  • Fecha de inicio del evento
    2010-10-04
  • Fecha de publicación del evento
    2011-02-23
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-06-21
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97213
  • 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
    Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
  • Causa
    Cook, inc. is recalling single, double, triple, and five-lumen central venous catheter trays and single and double lumen picc peripherally inserted central venous catheter trays. these kits and trays contain 0.9% sodium chloride injection usp 5 ml fill in 6 ml flush syringes that have been recalled by excelsior medical. during a routine test for syringe sterility, a possible integrity failure wa.
  • Acción
    Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form.
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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.

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