International safety notice

Discovery NM 630, Optima NM/CT 640, Discovery NM/CT 670 DR, Discovery NM/CT 670 Pro, Discovery NM/CT 670ES, NM 830, NM 830 DoD, NM/CT 850, NM/CT 860, NM/CT 870 CZT, NM/CT 870 DR. Fabricados entre diciembre de 2018 y junio de 2020.

Spain / AEMPS · ESP · Jan 11, 2021

Key facts

Title Discovery NM 630, Optima NM/CT 640, Discovery NM/CT 670 DR, Discovery NM/CT 670 Pro, Discovery NM/CT 670ES, NM 830, NM 830 DoD, NM/CT 850, NM/CT 860, NM/CT 870 CZT, NM/CT 870 DR. Fabricados entre diciembre de 2018 y junio de 2020.
Regulator Spain / AEMPS
Country ESP
Brand Discovery NM 630, Optima NM/CT 640, Discovery NM/CT 670 DR, Discovery NM/CT 670 Pro, Discovery NM/CT 670ES, NM 830, NM 830 DoD, NM/CT 850, NM/CT 860, NM/CT 870 CZT, NM/CT 870 DR. Fabricados entre diciembre de 2018 y junio de 2020.
Manufacturer GE Medical Systems Israel, Functional Imaging, Israel
Models FMI40891_FSN_SPANISH, 40891, 28023, CT870, 670ES, 64757, 2021-008, 35-37, 53188, 28022, 91.822.52.89
Event type Safety Notice
Date Jan 11, 2021

At a glance

  • No Recall
  • Yes Field safety notice
  • 1–9 Matching device models in FDA data
  • 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