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  • Device 3576
  • Manufacturer 3576
  • Event 3974
  • Implant 0
Safety Alert Or Field Safety Notices for HemosIL Plasminogen
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2016/001/029/292/019
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for Pixi
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2015/009/001/291/015
  • Event Date Posted
    2015-06-01
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for WM 28300 und WM 28400
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2018/007/003/291/032
  • Event Date Posted
    2018-07-02
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for OXYWAY
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2016/004/008/701/006
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for Medumat with the blue test bag
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2015/003/013/081/004
  • Event Date Posted
    2015-03-03
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for MEDUMAT Transport, MEDUMAT Standard and Standarda, MODUL...
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2019/003/019/291/003
  • Event Date Posted
    2019-02-18
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for Battery pack MEDUCORE Easy
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2017/002/016/291/011
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for ACQUITY UPLC Sample Organizer, IVD
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2017/004/007/299/018
  • Event Date Posted
    2017-04-10
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for Safe-T-Vue 6, Safe-T-Vue 10
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2016/002/023/292/015
  • Event Date Posted
    2016-02-18
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for MyLab Twice/Esaote/Esaote
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2016/007/011/291/002
  • Event Date Posted
    2016-03-10
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for Gscan Brio/Esaote/Esaote
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2016/007/011/291/001
  • Event Date Posted
    2016-04-18
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for UV Therapy System UV 7001
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2018/010/024/291/002
  • Event Date Posted
    2018-10-05
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for NIO Intraosseous Device
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2016/008/017/299/003
  • Event Date Posted
    2016-08-16
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for GORE TIGRIS® Vascular Stent
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2015/002/002/701/001
  • Event Date Posted
    2015-01-29
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for Conformable GORE® TAG® Thoracic Endoprosthesis
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2017/009/025/291/009
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for Vyntus BODY with Option Diffusion
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2017/012/019/228/007
  • Event Date Posted
    2017-11-30
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for AVEA Ventilator
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2015/004/028/131/001
  • Event Date Posted
    2015-04-21
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for Völker-Bett 2080
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2015/011/019/291/010
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for Nursing beds 2080, 2082, S 280, S 282
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2016/005/025/299/014
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for Tubing Sets for Hemodialysis / NovaLine®
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2018/005/002/601/001
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for BORRELIA VIRCLIA® IgG MONOTEST
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2018/002/005/291/019
  • Event Date Posted
    2018-01-26
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for Juno DRF
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2016/003/002/292/006
  • Event Date Posted
    2016-01-18
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for Apollo I DRFI EZ I EZ DRF; Clinodigit EVa, JunoDRF
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2016/001/022/291/001
  • Event Date Posted
    2016-01-15
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for Apollo / DRF/ EZ / EZ DRF; Clinodigit EVO, JunoDRF
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2016/012/028/701/006
  • Event Date Posted
    2016-12-27
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Extra notes in the data
Safety Alert Or Field Safety Notices for SWiTCH, Needle protected safety catheter
  • Type of Event
    Safety alert / Field Safety Notice
  • Event ID
    2017/001/016/299/001
  • Event Date Posted
    2017-01-10
  • Event Country
    United Kingdom
  • Event Source
    MHRA
  • Notes / Alerts
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • 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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