Events

Field Safety Notices about False CE Marking on Syringe

According to Health Products Regulatory Authority, this field safety notices involved a device in Ireland that was produced by N/A.

What is this?

Field safety notices are communications sent out by medical device manufacturers or their representatives in relation to actions that they may be taking in relation to their product that is on the market. These are mainly for health workers, but also for users. They can include recalls and alerts.

Learn more about the data here
  • Type of Event
    Field Safety Notice
  • Event Number
    SN2002(01)
  • Date
    2002-03-21
  • Event Country
    Ireland
  • Event Source
    HPRA
  • Event Source URL
    http://www.hpra.ie/homepage/medical-devices/safety-information/safety-notices/item?t=/false-ce-marking-on-syringe&id=4196f825-9782-6eee-9b55-ff00008c97d0
  • Notes / Alerts
    "Irish data is current through April 2019. All of the data comes from the Health Products Regulatory Authority (Ireland), 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 data from the U.S. and Ireland."
  • Extra notes in the data
  • Reason
    R-d ject syringe  - a device with a false ce mark.
  • Action
    Please ensure that those responsible for the purchase of syringes are made aware of this issue.

Device

False CE Marking on Syringe
  • Model / Serial
  • Product Description
    False CE Marking on Syringe
  • Manufacturer
    N/A

Manufacturer

N/A
  • Source
    HPRA