International safety notice

Urgent Field Safety Notice for CARESCAPE-Beatmungsmodule E-sCO, E-sCOV, E-sCAiO, E-sCAiOV, E-sCAiOE, E-sCAiOVE by GE Healthcare Finland Oy

Germany / BfArM · DEU · Nov 22, 2019

Key facts

Title Urgent Field Safety Notice for CARESCAPE-Beatmungsmodule E-sCO, E-sCOV, E-sCAiO, E-sCAiOV, E-sCAiOE, E-sCAiOVE by GE Healthcare Finland Oy
Regulator Germany / BfArM
Country DEU
Brand CARESCAPE-Beatmungsmodule E-sCO, E-sCOV, E-sCAiO, E-sCAiOV, E-sCAiOE, E-sCAiOVE
Manufacturer GE Healthcare Finland Oy
Models SGV19264031HA, SGV19291040HA, SGV19294022HA, SGV19240376HA, SGV19270018HA, SGV19271137HA, SGV19260091HA, SGV19269302HA, SGV17321155HA, SGV19269308HA, SGV19260093HA, SGV19250089HA and 780 more
Date Nov 22, 2019
Regulator page bfarm.de

At a glance

  • No Recall
  • No 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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