International safety notice

Urgent Field Safety Notice for Quadrox-i/-iD | VHK 11000 by Maquet Cardiopulmonary GmbH

Germany / BfArM · DEU · Mar 31, 2023

Key facts

Title Urgent Field Safety Notice for Quadrox-i/-iD | VHK 11000 by Maquet Cardiopulmonary GmbH
Regulator Germany / BfArM
Country DEU
Brand Quadrox-i/-iD | VHK 11000
Manufacturer Maquet Cardiopulmonary GmbH
Models 701070445, 701070392, 04058863019178, 701073018, 04058863002125, 701067859, 04058863154411, 701070444, 50000, 04058863153599, 70000-J, 04058863153797 and 146 more
Date Mar 31, 2023
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 1,000+ Matching device models in FDA data
  • 1,000+ 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