Drug recall
Magnus Hybrid OR Table Column (1180.01B2) used in conjunction with Siemens Artis Zeego Angiography System…
FDA recall event 71446 · Class II · Maquet Cardiovascular Us Sales, Llc
Key facts
| Event ID | 71446 |
|---|---|
| Recall numbers | Z-2097-2015 |
| Recalling firm | Maquet Cardiovascular Us Sales, Llc |
| Product type | Devices |
| Products | Magnus Hybrid OR Table Column (1180.01B2) used in conjunction with Siemens Artis Zeego Angiography System. Maquet GmbH & Co. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | There is a potential issue that could result to collision between the C-arm of the angiography system and the MAGNUS OR table system. After switching on the angiography-system, in rare cases, MAGNUS… |
| Initiation date | Jun 10, 2015 |
| Report date | Jul 29, 2015 |
| Termination date | Apr 18, 2016 |
| City | Wayne |
| State | NJ |
| Country | United States |
| FEI number | 3008355164 |
At a glance
- 1–9 Products in this recall
- 1–9 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: