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Bebig Isotopentechnik Gmbh recalls SagiPlan 2.2, CE0344, Rx Only , Brachyterapy Treatment Planning System
Recalled December 20, 2023 · FDA recall Z-0517-2024 · Bebig Isotopentechnik
Hazard
Due to software malfunction, numerical values may be rounded resulting in inaccurate measurements. · FDA Class II
Units
2 software licenses in US, 255 software licenses in OUS
Sold at
US: MD OUS: Germany
Description
Due to software malfunction, numerical values may be rounded resulting in inaccurate measurements.
Product
SagiPlan 2.2, CE0344, Rx Only , Brachyterapy Treatment Planning System
Manufacturer(s)
Bebig Isotopentechnik Gmbh
Made in
Germany
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →