Drug recall
AGFA DX-D 100 is a mobile digital radiography x-ray system
FDA recall event 71393 · Class II · AGFA Healthcare Corp.
Key facts
| Event ID | 71393 |
|---|---|
| Recall numbers | Z-1745-2015 |
| Recalling firm | AGFA Healthcare Corp. |
| Product type | Devices |
| Products | AGFA DX-D 100 is a mobile digital radiography x-ray system |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | When using the DX-D 100 unit, sporadic unintended movements caused by an electrostatic discharge of the unit to the ground may occur. |
| Initiation date | May 29, 2015 |
| Report date | Jun 17, 2015 |
| Termination date | Jan 18, 2017 |
| City | Greenville |
| State | SC |
| Country | United States |
| FEI number | 3001236302 |
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: