International safety notice

Urgent Field Safety Notice for Artis zee/Q/Q.zen systems by Siemens Healthcare GmbH Advanced Therapies

Germany / BfArM · DEU · Jul 6, 2021

Key facts

Title Urgent Field Safety Notice for Artis zee/Q/Q.zen systems by Siemens Healthcare GmbH Advanced Therapies
Regulator Germany / BfArM
Country DEU
Brand Artis zee/Q/Q.zen systems
Manufacturer Siemens Healthcare GmbH Advanced Therapies
Models 10848282, 64872105, AX044, AX045, 10848355, 10094137, 213821, 10848353, 10094141, 10848281, 10094139, 10094135 and 2 more
Date Jul 6, 2021
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 10–99 Matching device models 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

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