Drug recall
Artis one fluoroscopic x-ray system and patient table Artis one is an angiography system developed for…
FDA recall event 79538 · Class II · Siemens Medical Solutions USA, Inc
Key facts
| Event ID | 79538 |
|---|---|
| Recall numbers | Z-1148-2018 |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Product type | Devices |
| Products | Artis one fluoroscopic x-ray system and patient table Artis one is an angiography system developed for diagnostic imaging and interventional procedures including, but not limited to, pediatric and… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Certain patient table systems may have a missing or incorrectly installed snap ring that could cause the bolt to slide out of its base and the tabletop carriage to slide to the floor. |
| Initiation date | Jan 12, 2018 |
| Report date | Mar 28, 2018 |
| Termination date | Aug 28, 2018 |
| 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
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Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: