International safety notice

EZ Glide Aortic Cannula

Ireland / HPRA · IRL · Nov 5, 2019

Key facts

Title EZ Glide Aortic Cannula
Regulator Ireland / HPRA
Country IRL
Brand EZ Glide Aortic Cannula
Manufacturer Edwards LifeSciences
Models 225885, 210111, 214961, 219212, 212035, 214717, 230690, 213506, 220151, 206776, 218457, 219561 and 114 more
Event type Recall
Date Nov 5, 2019
Regulator page hpra.ie

At a glance

  • Yes 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