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Recall Observatory FDA recall evidence

Device product

Focal SIM Planning of radiation therapy

Z-2002-2012

June 21, 2012

Class II

Product summary

Firm
Elekta, Inc.
Event
Event 62433
Status
Terminated
Classification
Class II
Quantity
38 units
Official record key
device-enforcement:Z-2002-2012

Official wording

Reason: Incorrect patient shift directions when the Setup reference dialog is printed out when the DICOM coordinates option is enabled for reports.

Code information: Version 4.64.00 - 4.700, inclusive

Distribution pattern: Nationwide Distribution including CA, CT, FL, IL, IN, KY, MI, MN, MO, NJ, NY, NC, OH, OK, OR, PA, WA, and WI.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Incorrect patient shift directions when the Setup reference dialog is printed out when the DICOM coordinates option is enabled for reports.