Drug recall
Multitom RAX with software version VF10
FDA recall event 87995 · Class II · Siemens Medical Solutions USA, Inc
Key facts
| Event ID | 87995 |
|---|---|
| Recall numbers | Z-1685-2021 |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Product type | Devices |
| Products | Multitom RAX with software version VF10 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA Requested |
| Reason for recall | Siemens identified two issues, In some cases, it is possible to perform an image acquisition although more than 20% of the beam does not hit the detector. This may only occur when an organ program for… |
| Initiation date | Apr 20, 2021 |
| Report date | Jun 9, 2021 |
| Termination date | Nov 8, 2023 |
| 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: