FDA Medical Device Recalls (openFDA)
Siemens Medical Solutions USA, Inc: Urology X-Ray System, Uroskop D1/D2/D3 - Hardware for Motor Drive
- Recall number
- Z-0009-04
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Product
- Urology X-Ray System, Uroskop D1/D2/D3 - Hardware for Motor Drive
- Status
- Terminated
- Initiated
- 2003-08-08
- Posted
- 2003-10-15
- Terminated
- 2004-01-16
- Reason
- possible movement of table tilt and table longitudinal
- Root cause
- Other
- Action
- 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.
- Quantity
- 34 units
- Distribution
- Nationwide. The product was shipped to medical facilities in CA, FL, GA, IL, MD, NC, NJ, NY, OK, PA, SC, TN, TX, VA, WI, and WV.
- Lot, serial or model codes
- Uroskop D1/D2/D3
- 510(k) numbers
- ["K923049"]
- PMA numbers
- not on file
- Product code
- JAA
- Firm FEI
- 2240869
- Firm city
- Malvern
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28