Siemens Medical Solutions, USA, Inc Siemens KinetDx 4.2 Workplace, Siemens Medical Solutions, Ann Arbor, MI; 10090235. Indicated for use by the physician to aid in diagnosis, and by medical professionals whenever they would require or desire access to medical images and patient demographic information. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Siemens KinetDx 4.2 Workplace, Siemens Medical Solutions, Ann Arbor, MI; 10090235. Indicated for use by the physician to aid in diagnosis, and by medical professionals whenever they would require or desire access to medical images and patient demographic information.
Brand
Siemens Medical Solutions, USA, Inc
Lot Codes / Batch Numbers
All units.
Products Sold
All units.
Siemens Medical Solutions, USA, Inc is recalling Siemens KinetDx 4.2 Workplace, Siemens Medical Solutions, Ann Arbor, MI; 10090235. Indicated for us due to If the text is manually modified and additional phrases added as a result of worksheet interactions, some of the phrases may not populate the report.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
If the text is manually modified and additional phrases added as a result of worksheet interactions, some of the phrases may not populate the report.
Recommended Action
Per FDA guidance
Consignees were notified of the problem via a Customer Safety Advisory Notice dated 7/23/08, which provided guidance on how to minimize the risk of the problem occurring, and told customers that a service patch will be installed when it becomes available.
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