Drug recall
Ysiosystem with VC10 software version, Model Number 10281013. Radiographic system
FDA recall event 89703 · Class II · Siemens Medical Solutions USA, Inc
Key facts
| Event ID | 89703 |
|---|---|
| Recall numbers | Z-0841-2022 |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Product type | Devices |
| Products | Ysiosystem with VC10 software version, Model Number 10281013. Radiographic system |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Siemens Healthineers has identified a software error in previous software version VB10 for the Ysio fully automated system. The unit may process incorrect internal values for the position of its… |
| Initiation date | Jan 31, 2022 |
| Report date | Apr 6, 2022 |
| 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: