Drug recall
Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number: 10094137
FDA recall event 87672 · Class II · Siemens Medical Solutions USA, Inc
Key facts
| Event ID | 87672 |
|---|---|
| Recall numbers | Z-1495-2021 |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Product type | Devices |
| Products | Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number: 10094137 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Some Artis zee ceiling systems show an increased abrasion of the cabling at the cable outlet of the inner C-arm, the limited functionality may not be sufficient to continue with treatment as planned… |
| Initiation date | Mar 26, 2021 |
| Report date | May 5, 2021 |
| 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: