International safety notice

GE Healthcare

United Kingdom / MHRA · GBR · Nov 15, 2021

Key facts

Title GE Healthcare
Regulator United Kingdom / MHRA
Country GBR
Brand Centricit High Acuity Anaesthesia/Critical Care
Manufacturer GE Healthcare
Models 5.2.0.1.1-1134, 5.3.0.2.1-1044, 5.6.0.2.1-1520, 5.1.0.1.3-1200, 38008, 5.1.0.3.1-1277, 5.6.0.0.3-1345, 5.4.0.1.2-1542, 5.5.0.1.1-1341, 5.6.0.1.2-1495, 53188, 5.2.0.0.4-1026 and 6 more
Event type Safety Notice
Action type Field safety notice
Date Nov 15, 2021
Regulator page gov.uk

At a glance

  • No Recall
  • Yes Field safety notice

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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