International safety notice

Urgent Field Safety Notice for AFX EndoVascular AAA System by Endologix International Holdings B.V.

Germany / BfArM · DEU · Nov 17, 2017

Key facts

Title Urgent Field Safety Notice for AFX EndoVascular AAA System by Endologix International Holdings B.V.
Regulator Germany / BfArM
Country DEU
Brand AFX EndoVascular AAA System
Manufacturer Endologix International Holdings B.V.
Models F00382, F00641, F00726-11, F00416, F00645, F00415, I20-13, BA28-70, F00412, F00726-05, F00703-06, BA25-70 and 148 more
Date Nov 17, 2017
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 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