Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SagiPlan 2.2 Recalled by Bebig Isotopentechnik Gmbh Due to Due to software malfunction, numerical values may be...
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 Bebig Isotopentechnik Gmbh directly.
Affected Products
SagiPlan 2.2, CE0344, Rx Only , Brachyterapy Treatment Planning System
Quantity: 2 software licenses in US, 255 software licenses in OUS
Why Was This Recalled?
Due to software malfunction, numerical values may be rounded resulting in inaccurate measurements.
Where Was This Sold?
This product was distributed to 1 state: MD
About Bebig Isotopentechnik Gmbh
Bebig Isotopentechnik Gmbh 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