International safety notice
Possible inadvertent deletion of accessory elements (including dynamic MLC) in VARIS Vision, Varian medical systems
Germany / BfArM · DEU · Jun 17, 2011
Key facts
| Title | Possible inadvertent deletion of accessory elements (including dynamic MLC) in VARIS Vision, Varian medical systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Possible inadvertent deletion of accessory elements (including dynamic MLC) in VARIS Vision, Varian medical systems |
| Manufacturer | Possible inadvertent deletion of accessory elements (including dynamic MLC) in VARIS Vision, Varian medical systems |
| Models | H831019, H832181, 75081, H833955, H834293, H833686, H836168, H833956, H838433, CH-6303, H836485, H837058 and 461 more |
| Date | Jun 17, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 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