International safety notice

Smith's Medical (Portex)

United Kingdom / MHRA · GBR · Feb 11, 2019

Key facts

Title Smith's Medical (Portex)
Regulator United Kingdom / MHRA
Country GBR
Brand Portex® Blue Line Ultra® Tracheostomy Tubes
Manufacturer Smith's Medical (Portex)
Models 3651082, 3646833, 306701, 3635765, 55442, 3646828, 3646829, 3646830, 3639446, 3642834, 3646832, 3646831
Event type Recall, Safety Notice
Action type Field safety notice
Date Feb 11, 2019
Regulator page gov.uk

At a glance

  • Yes Recall
  • Yes Field safety notice

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