Drug recall
Ysio, model no. 10281013 Product Usage: The product is a stationary X-Ray system.
FDA recall event 85029 · Class II · Siemens Medical Solutions USA, Inc
Key facts
| Event ID | 85029 |
|---|---|
| Recall numbers | Z-1501-2020 |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Product type | Devices |
| Products | Ysio, model no. 10281013 Product Usage: The product is a stationary X-Ray system. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The Ysio system may process incorrect internal values for the position of its ceiling tube stand. If in this situation the user activates longitudinal or transversal stand movement (by using the… |
| Initiation date | Feb 10, 2020 |
| Report date | Mar 25, 2020 |
| Termination date | Aug 31, 2020 |
| 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: