International safety notice

Urgent Field Safety Notice for Heater Unit HU 35, Rotaflow System, Rotaflow Systtem with Rotaflow ICU Console by Maquet Cardiopulmonary GmbH

Germany / BfArM · DEU · Oct 28, 2020

Key facts

Title Urgent Field Safety Notice for Heater Unit HU 35, Rotaflow System, Rotaflow Systtem with Rotaflow ICU Console by Maquet Cardiopulmonary GmbH
Regulator Germany / BfArM
Country DEU
Brand Heater Unit HU 35, Rotaflow System, Rotaflow Systtem with Rotaflow ICU Console
Manufacturer Maquet Cardiopulmonary GmbH
Models 94175495, 94175552, 94175454, 94175492, 94175506, 90032386, 90032397, 94175531, 94175467, 90032320, 94175476, 90032267 and 289 more
Date Oct 28, 2020
Regulator page bfarm.de

At a glance

  • No Recall
  • No 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

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