International safety notice

Urgent Field Safety Notice for Philips Azurion, Philips Allura by Philips Medical Systems Nederland B.V.

Germany / BfArM · DEU · Feb 11, 2025

Key facts

Title Urgent Field Safety Notice for Philips Azurion, Philips Allura by Philips Medical Systems Nederland B.V.
Regulator Germany / BfArM
Country DEU
Brand Philips Azurion, Philips Allura
Manufacturer Philips Medical Systems Nederland B.V.
Models 722234, 722011, 722058, ALLURAXPERFD20, 722226, 722012, 722231, 722078, FCO72200554, 722023, 722228, 722225 and 42 more
Date Feb 11, 2025
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