Drug recall
SOMATOM Perspective, Computed tomography x-ray system
FDA recall event 75860 · Class II · Siemens Medical Solutions USA, Inc
Key facts
| Event ID | 75860 |
|---|---|
| Recall numbers | Z-0919-2017, Z-0920-2017, Z-0921-2017 |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Product type | Devices |
| Products | SOMATOM Perspective, Computed tomography x-ray system, SOMATOM Scope, Computed tomography x-ray system, SOMATOM Scope Power, Computed tomography x-ray system |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Siemens is providing a new installation of the Residual Current Monitor (RCM) in the Line Connection Box (LCB) to resolve a potential defect that could lead to a power cutout during use of the SOMATOM… |
| Initiation date | Nov 22, 2016 |
| Report date | Jan 4, 2017 |
| Termination date | May 30, 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: