International safety notice
Unintended Plan Modifications in Acuity or VARiS from Varian
Germany / BfArM · DEU · Nov 22, 2005
Key facts
| Title | Unintended Plan Modifications in Acuity or VARiS from Varian |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Unintended Plan Modifications in Acuity or VARiS from Varian |
| Manufacturer | Unintended Plan Modifications in Acuity or VARiS from Varian |
| Models | 827-4265, VARIAN5, 7.3.10, CP-2005-021, FAX-408-321-4499, 888-VARIAN5 |
| Date | Nov 22, 2005 |
| 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