Siemans Medial Solutions USA, Inc Acuson Cypress Echocardiography System. Imaging System Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Acuson Cypress Echocardiography System. Imaging System
Brand
Siemans Medial Solutions USA, Inc
Lot Codes / Batch Numbers
Catalog # 8264604. Serial numbers 70000 through 72000.
Products Sold
Catalog # 8264604. Serial numbers 70000 through 72000.
Siemans Medial Solutions USA, Inc is recalling Acuson Cypress Echocardiography System. Imaging System due to software problem - loss of data. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
software problem - loss of data
Recommended Action
Per FDA guidance
The recalling firm issued a letter dated 4/03 explaining the problem and the work around. A software upgarde is being provided free of charge to the customers.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026