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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 - Under certain circumstances, the portal image may be overwritten, which may lead to incorrect dosage.
Incorrect measurement of the aortic length in certain cases of aneurysm during the use of the aorta protocol or customized protocol of the Centricity AW Suite 2.0 running on the Centricity RA 1000 or RA600/CA1000 workstations.
A software anomaly results in incorrect study date and time information being displayed in the report screen and title, which may result in a potential patient misdiagnosis.