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All product recalls associated with Siemens Medical Solutions USA, Inc..
Total Recalls
613
Past Year
25
Class I (Serious)
0
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.
The product assembly can cause a failure of the transducer which results in a double and/or overlapped image which may ultimately result in misleading or false information, inability to accurately diagnose, incorrect positioning/locating/insertion of the biopsy needle and/or an interruption during the biopsy procedure.
System may either display incorrect mechanical and thermal index values, or fail to display them altogether.
Software - Under certain circumstances, the portal image may be overwritten, which may lead to incorrect dosage.