Drug recall
Mavig Monitor Suspension System, Model GD60, contained in the following Fluoroscopic imaging systems: Advantx…
FDA recall event 72966 · Class II · GE Medical Systems, LLC
Key facts
| Event ID | 72966 |
|---|---|
| Recall numbers | Z-0763-2016 |
| Recalling firm | GE Medical Systems, LLC |
| Product type | Devices |
| Products | Mavig Monitor Suspension System, Model GD60, contained in the following Fluoroscopic imaging systems: Advantx LCV+, Advantx LCN+, Advantx LCLP+, Advantx LCA, INNOVA 2000, INNOVA 4100, INNOVA 3100… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | GE Healthcare has recently become aware of a reported incident in which a Mavig suspension arm with monitor assembly fell to the floor. |
| Initiation date | Dec 18, 2015 |
| Report date | Feb 17, 2016 |
| Termination date | Sep 7, 2016 |
| City | Waukesha |
| State | WI |
| Country | United States |
| FEI number | 2126677 |
At a glance
- 1–9 Products in this recall
- 10–99 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: