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All product recalls associated with Siemens Medical Solutions USA, Inc.
Total Recalls
882
Past Year
41
Class I (Serious)
2
Most Recent
Dec 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
A software bug may lead to one image to be assigned to two different patients, which could potentially affect medical diagnosis.
Two software issues (1) Using the override function in case of blocked system movements affecting Luminos dRF Max, Luminos Agile Max and Uroskop Omnia Max systems may cause collision of the system under operator control with obstacles or persons .(2) Incorrectly assigned image affecting Ysio Max, Luminos dRF Max and Luminos Agile Max systems with detector MAX Static causing incorrect base for diagnosis
A software error is causing the analyzer to incorrectly eject affected Humidity Packs as expired.