International safety notice

Safety Notice for GE Anesthesia Devices, GE Healthcare

Germany / BfArM · DEU · Jan 22, 2014

Key facts

Title Safety Notice for GE Anesthesia Devices, GE Healthcare
Regulator Germany / BfArM
Country DEU
Brand GE Anesthesia Devices, GE Healthcare
Manufacturer Safety Notice for GE Anesthesia Devices, GE Healthcare
Models M1150345, M1204616, 1006-0402-000, 1009-0632-000, 10921417, M1116146, 2067226-001, M1132382, 1006-0939-000, 1006-0959-000, M1205870, M1156637 and 11 more
Date Jan 22, 2014
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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