International safety notice

Urgent Field Safety Notice for AXIOM Multix MT/MP/Swing/Top, Vertix MD/Solitaire by Siemens Healthcare GmbH, X-Ray Products (XP)

Germany / BfArM · DEU · May 28, 2024

Key facts

Title Urgent Field Safety Notice for AXIOM Multix MT/MP/Swing/Top, Vertix MD/Solitaire by Siemens Healthcare GmbH, X-Ray Products (XP)
Regulator Germany / BfArM
Country DEU
Brand AXIOM Multix MT/MP/Swing/Top, Vertix MD/Solitaire
Manufacturer Siemens Healthcare GmbH, X-Ray Products (XP)
Models 8395399, 475509, 213821, 475517, 8395431, APR23, 8395381, 8395415, 27.000, 27GMT, DE64872105, 91052 and 5 more
Date May 28, 2024
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 Matching device models in FDA data
  • 1–9 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