Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
COMPASS SW Version 3.1 Recalled by Iba Dosimetry Gmbh Due to Error in the software. During internal tests of...
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 Iba Dosimetry Gmbh directly.
Affected Products
COMPASS SW Version 3.1, Catalog Number CS10-100, medical linear accelerator, radiological
Quantity: 124 units
Why Was This Recalled?
Error in the software. During internal tests of the current development version of the Compass SW it was found that dose reconstruction for DMLC plans when the jaws move or mlc leaves reverse during beam on will not be scaled correctly for all control points.
Where Was This Sold?
This product was distributed to 2 states: AZ, OK
About Iba Dosimetry Gmbh
Iba Dosimetry Gmbh has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report