Siemens Medical Solutions USA, Inc Powermobil Mobile X-Ray System Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Powermobil Mobile X-Ray System
Brand
Siemens Medical Solutions USA, Inc
Lot Codes / Batch Numbers
Model number 2830011
Products Sold
Model number 2830011
Siemens Medical Solutions USA, Inc is recalling Powermobil Mobile X-Ray System due to Screws may become loose and fall into the OR field during surgery.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Screws may become loose and fall into the OR field during surgery.
Recommended Action
Per FDA guidance
The recalling firm has their Service Engineers visiting each site to check the screws on the window and secure them with Loctite per Update Instructions SP022/05/S. The Service Engineer is also informing the account of the problem during the visits.
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