Plan Parameters workspace within Eclipse Treatment Planning System Version 11 and 13
Medical device recall Z-0552-2014. Published in FDA’s Enforcement Report on Jan 1, 2014.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Jan 1, 2014. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Not named no state, in where it went
- 6701 how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
An anomaly has been traced to a software deficiency within the Plan Parameters workspace. When a dose relevant parameter is changed and “do no clear MUs and Reference Point dose” is selected, the Monitor units may change.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Plan Parameters workspace within Eclipse Treatment Planning System Version 11 and 13; ARIA Radiation Oncology versions 11 and 13 Acuity, versions 11 and 13. Manufactured by Varian Medical Systems Palo Alto, CA. Used in radiation therapy simulation.
6701, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Model numbers H48, HIT, H77: Code numbers: H480001 H480164 H480362 H480544 H480717 H480969 H481133 H481323 H481504 H48179S H481969 H482027 H48208S H480004 H48016S H48036S H48054S H48072S H480972 H481134 H481326 H481SOS H481796 H481970…
Every code shown here, 1,995 characters
Model numbers H48, HIT, H77: Code numbers: H480001 H480164 H480362 H480544 H480717 H480969 H481133 H481323 H481504 H48179S H481969 H482027 H48208S H480004 H48016S H48036S H48054S H48072S H480972 H481134 H481326 H481SOS H481796 H481970 H482028 H482086 H480009 H480174 H480373 H480546 H480727 H480974 H481138 H481327 H481506 H481804 H481971 H482029 H482087 H480010 H480175 H480374 H480547 H480760 H480975 H48114S H481328 H481510 H48180S H481972 H482030 H482088 H480011 H480176 H480378 H480548 H480764 H480980 H481146 H481329 H48152S H481806 H481973 H482031 H482089 H48001S H480181 H480379 H480566 H480765 H480981 H481147 H481334 H481532 H481807 H481974 H482032 H482090 H480030 H480182 H480380 H480578 H480766 H480989 H481148 H48133S H481533 H481815 H481975 H482033 H482091 H480033 H480200 H480381 H480579 H480767 H480992 H481153 H481343 H481540 H481816 H481976 H482034 H482092 H480034 H480207 H480382 H480580 H480769 H480994 H481154 H481352 H481543 H481834 H481977 H482035 H482093 H480035 H480208 H480384 H480581 H480770 H480996 H481155 H481353 H481544 H481835 H481978 H482036 H482094 H480036 H480209 H480404 H480582 H480774 H480997 H481156 H481354 H481545 H481836 H481979 H482037 H482095 H480037 H480210 H480405 H480590 H480782 H480998 H481164 H4813SS H481581 H481837 H481980 H482038 H482096 H480038 H480219 H480408 H480591 H480785 H480999 H481165 H481358 H481582 H481838 H481981 H482039 H482097 H480039 H480222 H480409 H480593 H480786 H481000 H481166 H481359 H481583 H481843 H481982 H482040 H482098 H480043 H480223 H480410 H480610 H480787 H481005 H481168 H481360 H481587 H481846 H481983 H482041 H482099 H480044 H480224 H480422 H480626 H480794 H481006 H481171 H481376 H481601 H481847 H481984 H482042 H482100 H48004S H48022S H48042S H480632 H480795 H481007 H481172 H481414 H481610 H481850 H481985 H482043 H482101 H480051 H480226 H480427 H480633 H480803 H481008 H481176 H481415 H481611 H481851 H481986 H482044 H482102 H480052 H480227 H480428 H480634 H480804 H481009 H481177 H481416 H481612 H481852…
FDA’s list runs to 54,030 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Worldwide Distribution.
These words name no state.
The words say it went outside the United States too.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Nov 18, 2013.
- FDA classified it on Dec 20, 2013.
- FDA’s Enforcement Report published it on Jan 1, 2014.
- FDA terminated it on Mar 13, 2015.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Varian Medical Systems, Inc., of Palo Alto, CA.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 54,030 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.