Siemens Uroskop Access — Class II medical device recall Z-2341-2012
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2012-09-19, distributed nationwide. Siemens has discovered a possible hazard to patients or hospital personnel when tilting the Uroskop Access sys
| Recall number | Z-2341-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions USA, Inc, Malvern, PA, United States |
| Recall initiated | 2012-04-30 |
| Classified | 2012-09-10 |
| Reported by FDA | 2012-09-19 |
| Terminated | 2012-09-20 |
| Distributed | Nationwide (US) |
| Quantity | 5 |
| Serial numbers | 6076, 6078, 6080, 6081, 6082 |
| Model numbers | 5756130 |
Product
Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2341-2012. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.