International safety notice

Safety Notice for the Discovery NM/CT 670 SPECT/CT and Discovery NM 630 SPECT Systems, GE Healthcare

Germany / BfArM · DEU · Oct 25, 2012

Key facts

Title Safety Notice for the Discovery NM/CT 670 SPECT/CT and Discovery NM 630 SPECT Systems, GE Healthcare
Regulator Germany / BfArM
Country DEU
Brand the Discovery NM/CT 670 SPECT/CT and Discovery NM 630 SPECT Systems, GE Healthcare
Manufacturer Safety Notice for the Discovery NM/CT 670 SPECT/CT and Discovery NM 630 SPECT Systems, GE Healthcare
Models 40846, 53226, FMI40846_FSN_ENGLISH, NM630
Date Oct 25, 2012
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 Matching device models 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