Drug recall
GE Healthcare Revolution CT., multi-slice (256 detector row) CT scanner.
FDA recall event 70074 · Class II · GE Healthcare
Key facts
| Event ID | 70074 |
|---|---|
| Recall numbers | Z-0985-2015 |
| Recalling firm | GE Healthcare |
| Product type | Devices |
| Products | GE Healthcare Revolution CT., multi-slice (256 detector row) CT scanner. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Potential safety issue due to a required torque check on three bolted joints of the Revolution CT scanner. No injuries or illnesses reported. |
| Initiation date | Dec 19, 2014 |
| Report date | Jan 21, 2015 |
| Termination date | Apr 29, 2015 |
| 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: