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All product recalls associated with Siemens Medical Solutions USA, Inc.
Total Recalls
1000
Past Year
49
Class I (Serious)
29
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.
Software issue. Allows for users to enter date in Pre-Cath Holding Area prior to registering the patient in the Cath Lab.
The marker band in guidewire lumen could move from the manufactured location during clinical use.
Recalling firm became aware of a potential problem through the submission of a product complaint to the firm reporting the Image Navigator feature in the MagicView 300 VA42A or VA42B software are not being imported accurately to certain CT or MR images.