International safety notice

Urgent Field Safety Notice for Discovery NM 630, Optima NM/CT 640, Discovery NM/CT 670 DR, Discovery NM/CT 670 Pro, Discovery NM/CT 670 ES, NM 830, NM 830 DoD, NM/CT 850, NM/CT 860, NM/CT 870 CZT, NM/CT 870 DR by GE Medical Systems Israel, Functional Imaging

Germany / BfArM · DEU · Jan 11, 2021

Key facts

Title Urgent Field Safety Notice for Discovery NM 630, Optima NM/CT 640, Discovery NM/CT 670 DR, Discovery NM/CT 670 Pro, Discovery NM/CT 670 ES, NM 830, NM 830 DoD, NM/CT 850, NM/CT 860, NM/CT 870 CZT, NM/CT 870 DR by GE Medical Systems Israel, Functional Imaging
Regulator Germany / BfArM
Country DEU
Brand Discovery NM 630, Optima NM/CT 640, Discovery NM/CT 670 DR, Discovery NM/CT 670 Pro, Discovery NM/CT 670 ES, NM 830, NM 830 DoD, NM/CT 850, NM/CT 860, NM/CT 870 CZT, NM/CT 870 DR
Manufacturer GE Medical Systems Israel, Functional Imaging
Models 40891_FSN_ENGLISH, 40891, 670ES
Date Jan 11, 2021
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

Browse all International device safety notices