Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Siemens syngo WorkFlow SLR Recalled by Siemens Medical Solutions USA, Inc Due to Under certain conditions, when using the Search functionality,...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Siemens Medical Solutions USA, Inc directly.
Affected Products
Siemens syngo WorkFlow SLR, Radiological Information System, Version VA31A SP1/SP2/SP3 The information system syngo(R) Workflow SLR is a digital radiology information system (RIS) with integrated modules for patient administration, examination, reporting, statistics and system administration, as well as multiple interfaces for patient registration, order entry, and external billing modules. It is not intended to treat disease or administer any medicinal substances or drugs. There is no contact between device and patient. syngo(R) Workflow SLR can be used as a separate RIS, interfacing to a Hospital Information System (HIS) or Picture Archiving and Communication Systems (PACS
Quantity: 37
Why Was This Recalled?
Under certain conditions, when using the Search functionality, the potential exists for the wrong patient's Interactive Documents to display when viewing a signed report in the single patient view. This can occur when the Interactive Document is viewed or auto displayed, dismissed by the user, and then a different patient and signed exam is selected in single patient view. The Notes Viewer will
Where Was This Sold?
This product was distributed to 31 states: AL, CA, CO, DE, FL, GA, HI, IL, IN, KS, KY, LA, MD, MA, MO, NE, NV, NH, NJ, NY, NC, OH, OR, PA, TN, TX, VA, WV, WI, WY, DC
About Siemens Medical Solutions USA, Inc
Siemens Medical Solutions USA, Inc has 613 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report