Siemens Medical Solutions USA, Inc Urology X-Ray System, Uroskop D1/D2/D3 - Hardware for Motor Drive Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Urology X-Ray System, Uroskop D1/D2/D3 - Hardware for Motor Drive
Brand
Siemens Medical Solutions USA, Inc
Lot Codes / Batch Numbers
Uroskop D1/D2/D3
Products Sold
Uroskop D1/D2/D3
Siemens Medical Solutions USA, Inc is recalling Urology X-Ray System, Uroskop D1/D2/D3 - Hardware for Motor Drive due to possible movement of table tilt and table longitudinal. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
possible movement of table tilt and table longitudinal
Recommended Action
Per FDA guidance
The recalling firm issued Update Instructions SP016/03/S, SP017/03S and SP018/03/S that instruct the Service Engineers to visit each affected system to install the required parts.
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