Siemans Medial Solutions USA, Inc Acuson Cypress Echocardiography System Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Acuson Cypress Echocardiography System
Brand
Siemans Medial Solutions USA, Inc
Lot Codes / Batch Numbers
Catalog number 8264604, Serial numbers 73480 through 73535, 71165, 71561, 72532, 73125, and 73292.
Products Sold
Catalog number 8264604; Serial numbers 73480 through 73535, 71165, 71561, 72532, 73125, and 73292.
Siemans Medial Solutions USA, Inc is recalling Acuson Cypress Echocardiography System due to software problem - mode does not appear on screen. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
software problem - mode does not appear on screen
Recommended Action
Per FDA guidance
The recalling firm telephoned their direct accounts to inform them of the problem and the need to modify the software. The call were made from 2/2-16/04. The modification kits were sent to consignees via express delivery.
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 noticeDistribution
As reported by FDA
AZ, CA, CT, FL, IL, IN, IA, NE, NV, NY, OH, TX, WA
Page updated: Jan 10, 2026