International safety notice
Urgent field safety notice for eFilm Workstation/eFilm Lite versions 2.1 / 2.1.2 / 3.0 / 3.1 / 3.3.5 / 3.4 / 4.0 / 4.0.1 / 4.0.2 / 4.0.3 and 4.1, Merge Healthcare
Germany / BfArM · DEU · Jan 5, 2017
Key facts
| Title | Urgent field safety notice for eFilm Workstation/eFilm Lite versions 2.1 / 2.1.2 / 3.0 / 3.1 / 3.3.5 / 3.4 / 4.0 / 4.0.1 / 4.0.2 / 4.0.3 and 4.1, Merge Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | eFilm Workstation/eFilm Lite versions 2.1 / 2.1.2 / 3.0 / 3.1 / 3.3.5 / 3.4 / 4.0 / 4.0.1 / 4.0.2 / 4.0.3 and 4.1, Merge Healthcare |
| Manufacturer | Urgent field safety notice for eFilm Workstation/eFilm Lite versions 2.1 / 2.1.2 / 3.0 / 3.1 / 3.3.5 / 3.4 / 4.0 / 4.0.1 / 4.0.2 / 4.0.3 and 4.1, Merge Healthcare |
| Models | 1.1.3.1, 1.7.2, 1.1.1.1, 3.3.5, 2.1.2, 1.2.840, 1.7.3, 840.10008.5, 1.7.4, 1.1.2, 4.0.2, 1.7.1 and 14 more |
| Date | Jan 5, 2017 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 10–99 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