Siemens Medical Solutions USA, Inc Arcadis Orbic Mobile X-Ray System Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Arcadis Orbic Mobile X-Ray System
Brand
Siemens Medical Solutions USA, Inc
Lot Codes / Batch Numbers
model number 8081080
Products Sold
model number 8081080
Siemens Medical Solutions USA, Inc is recalling Arcadis Orbic Mobile X-Ray System due to patient information can be stored in another patient's file.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
patient information can be stored in another patient's file.
Recommended Action
Per FDA guidance
The recalling firm has issued a Customer Safety Advisory to the affected customers per Update Instructions SP030/05/S. The letter informs customers of the potential problem and provides a suggestion to avoid this issue.
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