International safety notice
Corrective action for the Discovery IGS 730 and Discovery IGS 740 angiography X-ray systems, GE Healthcare
Germany / BfArM · DEU · Jan 22, 2015
Key facts
| Title | Corrective action for the Discovery IGS 730 and Discovery IGS 740 angiography X-ray systems, GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Discovery IGS 730 and Discovery IGS 740 angiography X-ray systems, GE Healthcare |
| Manufacturer | Corrective action for the Discovery IGS 730 and Discovery IGS 740 angiography X-ray systems, GE Healthcare |
| Models | 203694IGS730, SO4242294, 53226, 10692VAS01, M4160476, YV2000, XR649425BU6, AE1477RX04, M40480222, 12223, SO4208228, 82416120043 and 14 more |
| Date | Jan 22, 2015 |
| 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