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Vista de la lista Vista de las tarjetas
  • Dispositivo 1
  • Fabricante 1
  • Evento 124969
  • Implante 0
Retiro De Equipo (Recall) de Engines for dental implant surgery
  • Tipo de evento
    Recall
  • ID del evento
    831
  • Fecha
    2018-05-18
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-08-18
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    Accepted 15-1317
Retiro De Equipo (Recall) de Computed tomography apparatus, computerized tomography apparatus
  • Tipo de evento
    Recall
  • ID del evento
    832
  • Fecha
    2018-04-18
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-11-23
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    Accepted 06-1250, Accepted 06-1251
Retiro De Equipo (Recall) de Therapeutic accelerators, therapeutic accelerators, therapeutic acce...
  • Tipo de evento
    Recall
  • ID del evento
    833
  • Fecha
    2018-04-19
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-11-24
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    Accepted 06-884, Accepted 02-40, Accepted 04-656, Accepted 08-232
Retiro De Equipo (Recall) de A universal ultrasound imaging apparatus, a general ultrasound imagi...
  • Tipo de evento
    Recall
  • ID del evento
    834
  • Fecha
    2018-04-18
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-09-07
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    No. 09-180, No. 04-1514, No. 09-209, No. 15-1089
Retiro De Equipo (Recall) de Medical reform apparatus (manual type)
  • Tipo de evento
    Recall
  • ID del evento
    835
  • Fecha
    2018-04-23
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-10-04
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    Seoul reception 07-1050
Retiro De Equipo (Recall) de Hemorrhoid Ringer
  • Tipo de evento
    Recall
  • ID del evento
    836
  • Fecha
    2018-04-19
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-11-22
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    Number 10-1085
Retiro De Equipo (Recall) de Diagnostic x-ray equipment
  • Tipo de evento
    Recall
  • ID del evento
    837
  • Fecha
    2018-04-23
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-09-01
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    Su-in 15-4014
Retiro De Equipo (Recall) de Epidural catheter
  • Tipo de evento
    Recall
  • ID del evento
    838
  • Fecha
    2018-04-24
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-10-24
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    Accepted 98-487
Retiro De Equipo (Recall) de Special material Fracture screw
  • Tipo de evento
    Recall
  • ID del evento
    839
  • Fecha
    2018-05-15
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-08-16
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    No. 13-1619
Retiro De Equipo (Recall) de Immunochemical test reagent
  • Tipo de evento
    Recall
  • ID del evento
    840
  • Fecha
    2018-04-24
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-09-01
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    No. 13-2096
Retiro De Equipo (Recall) de Hematology test reagent
  • Tipo de evento
    Recall
  • ID del evento
    841
  • Fecha
    2018-04-25
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-08-30
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    No. 13-3721
Retiro De Equipo (Recall) de Endoscope light source device
  • Tipo de evento
    Recall
  • ID del evento
    842
  • Fecha
    2018-04-26
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-10-05
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    Number 17-4487
Retiro De Equipo (Recall) de Gene sequence checker
  • Tipo de evento
    Recall
  • ID del evento
    843
  • Fecha
    2018-04-25
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-08-31
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    No. 16-145
Retiro De Equipo (Recall) de Load ECG device, biological signal processing device
  • Tipo de evento
    Recall
  • ID del evento
    844
  • Fecha
    2018-05-01
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-09-07
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    Su-in 04-418, Su-in 05-289
Retiro De Equipo (Recall) de Magnetic Resonance Computed Tomography System for Superconducting Ma...
  • Tipo de evento
    Recall
  • ID del evento
    845
  • Fecha
    2018-05-01
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-09-21
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    Su-in 14-2393
Retiro De Equipo (Recall) de Medical chemical sterilizer
  • Tipo de evento
    Recall
  • ID del evento
    846
  • Fecha
    2018-05-01
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-09-07
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    Su-in 15-4269
Retiro De Equipo (Recall) de Legal catheter cannula
  • Tipo de evento
    Recall
  • ID del evento
    847
  • Fecha
    2018-05-01
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-09-20
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    Number 06-317
Retiro De Equipo (Recall) de Secondary Healing Foam Wound Covers
  • Tipo de evento
    Recall
  • ID del evento
    848
  • Fecha
    2018-05-04
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-08-30
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    No. 12-1001
Retiro De Equipo (Recall) de Quality control material
  • Tipo de evento
    Recall
  • ID del evento
    859
  • Fecha
    2018-05-16
  • País del evento
    South Korea
  • Fecha de finalización del evento
    2018-09-26
  • Fuente del evento
    KFDA
  • URL de la fuente del evento
    https://emed.mfds.go.kr
  • Notas / Alertas
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and South Korea.
  • Notas adicionales en la data
    Seoul 13-2552
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