FDA Device recall Z-2341-2012
Siemens Uroskop Access
- FDA Device
- Class II
- terminated
- Published 2012-09-19
On 2012-09-19 the FDA classified a Class II recall of Siemens Uroskop Access by Siemens Medical Solutions Usa, citing siemens has discovered a possible hazard to patients or hospital personnel when tilting the Uroskop Access system starting with serial number 6076. When tilting the table on the U….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2341-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-04-30 |
| Published | 2012-09-19 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system
Reason
Siemens has discovered a possible hazard to patients or hospital personnel when tilting the Uroskop Access system starting with serial number 6076. When tilting the table on the Uroskop Access table, the motor may become disconnected and the entire table assembly may fall on the floor.
Identifiers
| code_info | Model number 5756130 -- serial numbers 6076, 6078, 6080, 6081, and 6082. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2341-2012%22
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