Drug recall
Siemens Artis zee Ceiling Systems. Angiographic x-ray system.
FDA recall event 67175 · Class II · Siemens Medical Solutions USA, Inc
Key facts
| Event ID | 67175 |
|---|---|
| Recall numbers | Z-1080-2014 |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Product type | Devices |
| Products | Siemens Artis zee Ceiling Systems. Angiographic x-ray system. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | During the lifetime of Artis zee Ceiling systems, there is an increased wear due to potential sub-optimal cable guidance that can lead to cable damage. |
| Initiation date | Dec 16, 2013 |
| Report date | Mar 5, 2014 |
| Termination date | Mar 9, 2015 |
| 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: