FDA Medical Device Recalls (openFDA)
Siemens Medical Systems Inc: Uroskop D1/D2/D3 - Table, Radiographic, Stationary Top.
- Recall number
- Z-0493-03
- Recalling firm
- Siemens Medical Systems Inc
- Product
- Uroskop D1/D2/D3 - Table, Radiographic, Stationary Top.
- Status
- Terminated
- Initiated
- 2002-11-27
- Posted
- 2003-01-30
- Terminated
- 2005-01-10
- Reason
- There is unintended system movement or unwanted automatic movement of the tabletop.
- Root cause
- Other
- Action
- Siemens personal will install Host Software VA00F and Generator Host Software VE00D on affected Uroskop units. Update instructions were sent to users November 27,2002 and December 7, 2002.
- Quantity
- 13
- Distribution
- Product was distributed to 6 hospitals nationwide and 5 government hospitals. Internationally, the tables were distributed to Germany, Netherlands, Italy , Luxembourg, Sweden, Austria, Switzerland, Slovakia, Hungary, Ukraine, Russia, Turkmenistan, South Africa, Canada, Malaysia, Japan, and Taiwan.
- Lot, serial or model codes
- Uroskop D1 -- Model #9785023 Uroskop D2/D3 -- Model #9785015
- 510(k) numbers
- ["K923049"]
- PMA numbers
- not on file
- Product code
- IXR
- Firm FEI
- 2240869
- Firm city
- Iselin
- Firm state
- NJ
- 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