International safety notice

Siemens

United Kingdom / MHRA · GBR · Jul 1, 2022

Key facts

Title Siemens
Regulator United Kingdom / MHRA
Country GBR
Brand AXIOM Sensis XP/ Sensis/ Sensis Lite/ Vibe Combo
Manufacturer Siemens
Models 11007642, 213821, 6623974, 10764562, 64872105, AX033, 6634641, 6634658, 6634633, 000006122, 10764561
Event type Safety Notice
Action type Field safety notice
Date Jul 1, 2022
Regulator page gov.uk

At a glance

  • No Recall
  • Yes Field safety notice
  • 1–9 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

Browse all International device safety notices