Events

Recall of ADULT NEBULIZER MASK

According to DPM Tunisie, this recall involved a device in Tunisia that was produced by YILKAL MEDICAL.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Date
    2015-07-13
  • Event Country
    Tunisia
  • Event Source
    DPMT
  • Event Source URL
    http://www.dpm.tn/
  • Notes / Alerts
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Extra notes in the data
    Country: Turkey

Device

ADULT NEBULIZER MASK

Manufacturer

YILKAL MEDICAL
  • Source
    DPMT