International safety notice
Correktive actions for Revolution XR/d and Definium 8000, GE Healtcare
Germany / BfArM · DEU · Apr 22, 2008
Key facts
| Title | Correktive actions for Revolution XR/d and Definium 8000, GE Healtcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Revolution XR/d and Definium 8000, GE Healtcare |
| Manufacturer | Correktive actions for Revolution XR/d and Definium 8000, GE Healtcare |
| Models | 5117866-2, 53188, 5117866-27, 5194381, 5272535-IEN-GB, 5147845-2J |
| Date | Apr 22, 2008 |
| 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