International safety notice

Recall for the Great Ormond Street GOS Tracheostomy Cannula Set, Teleflex Medical

Germany / BfArM · DEU · Dec 28, 2010

Key facts

Title Recall for the Great Ormond Street GOS Tracheostomy Cannula Set, Teleflex Medical
Regulator Germany / BfArM
Country DEU
Brand the Great Ormond Street GOS Tracheostomy Cannula Set, Teleflex Medical
Manufacturer Recall for the Great Ormond Street GOS Tracheostomy Cannula Set, Teleflex Medical
Models 7ÄEFIEX, 121001, 858813, 121002, 858812, 121003
Date Dec 28, 2010
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 10–99 Matching device models in FDA data
  • 10–99 Matching catalog numbers in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices