International safety notice

Maquet Cardiopulmonary (GETINGE)

United Kingdom / MHRA · GBR · Jul 31, 2020

Key facts

Title Maquet Cardiopulmonary (GETINGE)
Regulator United Kingdom / MHRA
Country GBR
Brand Product name listed in Annex 1 and comment section
Manufacturer Maquet Cardiopulmonary (GETINGE)
Models 94175489, 90032377, 94175452, 90032369, 90032399, 701046405, 90032367, 94175485, 90032406, 90032360, 90034556, 90032348 and 289 more
Event type Safety Notice
Action type Field safety notice
Date Jul 31, 2020
Regulator page gov.uk

At a glance

  • No Recall
  • Yes Field safety notice
  • 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