RegWardenFDA facility compliance records
Facility

C-RAD POSITIONING AB

3 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2018: 1 inspections; 2020: 1 recalls; 2025: 2 recalls2017120182019120202021202220232024220252026
  • Recalls (3)
  • Inspections (1)

Devices registered here (1)

Recalls & enforcement

  • Class IIOngoing2025-10-09
    Due to issues with the system's stereotactic radiosurgery (SRS) treatment cannot be guaranteed for all couch angles and system setups. n certain cases, the system may indicate the patient as correctly positioned at the isocenter, even when the isocenter is positioned outside of t…
  • Class IIOngoing2025-04-22
    Software issue with scanning equipment that can results in the filed rotation not being applied correctly.
  • Class IITerminated2020-08-06
    PC Application Software c4D not changing Site upon synchronization during the Setup workflow step

FDA inspections (1)

  • VAI2018-07-19
    Voluntary Action Indicated · Compliance: Devices; Radiation Control and Health Safety Act; Postmarket Assurance: Devices · citations posted

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “C-RAD POSITIONING AB (FEI 3006621300) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3006621300-c-rad-positioning-ab/

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