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  • Device 107
  • Manufacturer 107
  • Event 118
  • Implant 0
Safety Alert for 20 ml syringe
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for DAFILON®
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for HomeChoice system, HomeChoice Automated Peritoneal Dialysis System PRO
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for Volumetric infusion pumps
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for HOMECHOICE PERITONEAL DIALYSIS
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for Plasticat Peripheral Catheters known as Trocar
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for Central Venous Catheters
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for Coronary Angioplasty Guide, model: Galeo.
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for Coronary Angioplasty Guide, model: Galeo.
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for Coronary Angioplasty Guide, model: Galeo.
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for Galeo M 014 and F014
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for Galeo
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for Coronary Spirals Taxus or Stents
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for HeberFast Line Pregnancy II
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for UMELISA PSA
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for Therapeutic Ozonator, Model Ozomed-01
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for Biosensor SUMASENSOR SXT
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for Biosensor SUMASENSOR SXT
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for Fire Star™ RX and Dura Star™ RX PTCA
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for STEAM CONTROL
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for Table Autoclave, Model Vitale 21L
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for S / 5 Compact Monitors
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for Equipment for dental restoration
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for Doppler Transcraneal, Model EZ-Dop
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
Safety Alert for GIEMSA. Dye solution
  • Type of Event
    Safety alert
  • Event Country
    Cuba
  • Event Source
    HMC
  • Event Source URL
    https://www.cecmed.cu/vigilancia/equipos-medicos/alertas
  • Notes / Alerts
    Cuban data is current through 2018. All of the data comes from the Health Ministry of Cuba, 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 Cuba.
  • Extra notes in the data
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About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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