Drug recall
ARTISTE" MV System
FDA recall event 76712 · Class II · Siemens Medical Solutions USA, Inc
Key facts
| Event ID | 76712 |
|---|---|
| Recall numbers | Z-1488-2017, Z-1489-2017, Z-1490-2017, Z-1491-2017 |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Product type | Devices |
| Products | ARTISTE" MV System, Mevatron M2/Primus Mid-Energy PRIMUS HI, ONCOR" Avant-garde, ONCOR" Expression ONCOR" Impression ONCOR" Impression plus |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Software update |
| Initiation date | Feb 14, 2017 |
| Report date | Mar 29, 2017 |
| Termination date | Dec 18, 2017 |
| 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: