Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Software BeamAdjust version 2.2 Recalled by PTW NORTH AMERICA CORPORATION Due to When a measurement with a PTW detector array...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact PTW NORTH AMERICA CORPORATION directly.
Affected Products
Software BeamAdjust version 2.2, Catalog No: S070009 Software VeriSoft version 8.0, Catalog No: S080032
Quantity: 1 unit
Why Was This Recalled?
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
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About PTW NORTH AMERICA CORPORATION
PTW NORTH AMERICA CORPORATION has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report