TrueBeam Radiotherapy System 2.7Recalls & reported problems
Varian Medical Systems, Inc. · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00899475002233), received between Jun 17, 2022 and Jun 17, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Display or Visual Feedback Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Display or Visual Feedback Problem1
- Failure to Power Up1
- Output Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 17, 2022Display or Visual Feedback Problem; Failure to Power Up; Output Problem
REPORTS OVER THE COURSE OF THE PAST SIX MONTHS HAVE BEEN MADE TO VARIAN, TRUEBEAM'S MANUFACTURER, REGARDING THE MULTIPLE DOWNTIMES THE MACHINES HAVE BEEN EXPERIENCING WHICH HAS CAUSED THE CANCELLATION OF WELL OVER 100 DIFFERENT PATIENT'S RADIATION THERAPY FOR CANCER THERAPY. ISSUES INCLUDE DIFFICULTIES WITH THE DEVICES INTERNAL POWER SUPPLY, FAULT IN THE IMAGE STORING SERVER, AND FAULT IN THE COLLIMATOR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14732343 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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