Drug recall
Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system
FDA recall event 62988 · Class II · Siemens Medical Solutions USA, Inc
Key facts
| Event ID | 62988 |
|---|---|
| Recall numbers | Z-2341-2012 |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Product type | Devices |
| Products | Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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… |
| Initiation date | Apr 30, 2012 |
| Report date | Sep 19, 2012 |
| Termination date | Sep 20, 2012 |
| City | Malvern |
| State | PA |
| Country | United States |
| FEI number | 2240869 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: