Overview of recall records associated with Mobius Medical Systems, LP, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Mobius3D version 1.5.0 contained a defect in software code which affects users who perform beam customization, and may lead to a discrepancy in dose calculation between this version of…
This page summarizes recall records in which the official source identifies Mobius Medical Systems, LP as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
