Events

Recall of CH8 SUCTION CATHETER, CH10 SUCTION CATHETER AND CH12 SUCTION CATHETER

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

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
    2015-12-02
  • 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: CHINA

Device

CH8 SUCTION CATHETER, CH10 SUCTION CATHETER AND CH12 SUCTION CATHETER
  • Model / Serial
    20140710 (exp: 07/2019), 20140710 (exp: 07/2019) and 20140330 (exp: 03/2019)
  • Manufacturer
    NANTONG

Manufacturer

NANTONG
  • Source
    DPMT