Siemens Medical Solutions USA, Inc LANTIS XLINK (Impac MultiAccess Sequencer) on Varian accelerators with the MLC3PI interface Recall

Check Your Product

According to the U.S. Food and Drug Administration (FDA)

Reason for Recall

As stated by FDA

Improper treatment may be delivered if the machine configuration file is edited/set for the Varian MLC revision H file format.

Recommended Action

Per FDA guidance

The firm has issued a safety advisory letter to all affected consignees, and will distribute an updated software version as soon as it is available.