International safety notice

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

Germany / BfArM · DEU · Mar 10, 2022

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 10280959, 10848282, 10848280, 10848353, AX006, 10502503, AX004, 10502507, 10094141, 10094139, 213821, 10502505 and 16 more
Date Mar 10, 2022
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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