Lower riskMedical device recall · FDA · Published August 27, 2021
PTW Software BeamAdjust 2.2 and VeriSoft 8.0: Measurement error risk
PTW recalls software versions 2.2 and 8.0 for potential dose measurement errors affecting patient radiation therapy plans. Users should check their software versions and contact PTW for updates.
When a measurement with a PTW detector array is performed with the software BeamAdjust 2.2 or VeriSoft 8.0, a measurement error can occur under specific conditions. This error can lead to a too-low or too-high measured absolute dose which affects patient plan verification results
Take action
Contact the company
📍Recalling firmPTW NORTH AMERICA CORPORATION6 Mars Ct Rm Unit 5 · Boonton, NJ 07005-9309
“PTW Software BeamAdjust 2.2 and VeriSoft 8.0: Measurement error risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61882-ptw-software-beamadjust-2-2-and-verisoft-8-0-measurement. Based on FDA recall #Z-0479-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0479-2022%22&limit=1).
PTW NORTH AMERICA CORPORATION recalled BeamAdjust version 2.2 and VeriSoft version 8.0 software on Aug. 27, 2021, according to the FDA. The recall addresses measurement errors that can lead to incorrect absolute dose readings affecting patient plan verification.
How to tell if you have it
PTW BeamAdjust version 2.2, Catalog No: S070009
PTW VeriSoft version 8.0, Catalog No: S080032
The hazard
When a measurement with a PTW detector array is performed with the software BeamAdjust 2.2 or VeriSoft 8.0, a measurement error can occur under specific conditions. This error can lead to a too-low or too-high measured absolute dose which affects patient plan verification results.
Context
GovInfoNow's records show other recent recalls of similar products include RayStation/RayPlan Software Recall: Radiation Dose Calculation Errors (2025-11-28) and RayStation Software Recalls: Radiation Dose Calculation Errors in Some Regions (2025-11-28).
How to tell if you have this one
Check for software versions BeamAdjust 2.2 (Catalog No: S070009) or VeriSoft 8.0 (Catalog No: S080032) on PTW radiation therapy systems. The serial number AU2001094-1 and UDI EPTWS0700090 are associated with this recall.
Brand
PTW
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Software Version
Verify your BeamAdjust and VeriSoft versions to see if they match the recalled versions.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution in the state of CO.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 2.5 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0479-2022 (August 27, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0479-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.