International safety notice

Urgent Safety Notice for the Hemolung Cartridge Kit, ALung Technologies

Germany / BfArM · DEU · Jan 17, 2014

Key facts

Title Urgent Safety Notice for the Hemolung Cartridge Kit, ALung Technologies
Regulator Germany / BfArM
Country DEU
Brand the Hemolung Cartridge Kit, ALung Technologies
Manufacturer Urgent Safety Notice for the Hemolung Cartridge Kit, ALung Technologies
Models 010581, 1-412-697-3376, 15203, 010545, 010492, 010539, 010531, 0800-181-6344, 010543, 0-808-189-1190, 010466, 010482 and 53 more
Date Jan 17, 2014
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 100–999 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