Drug recall
DigitalDiagnost C50, Stationary X-ray System
FDA recall event 83654 · Class II · Philips Healthcare
Key facts
| Event ID | 83654 |
|---|---|
| Recall numbers | Z-2498-2019 |
| Recalling firm | Philips Healthcare |
| Product type | Devices |
| Products | DigitalDiagnost C50, Stationary X-ray System |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA Requested |
| Reason for recall | During recent evaluations of the Philips DigitalDiagnost C50 system, Philips identified a missing label. This notification is intended to provide you with information regarding what the issue is, and… |
| Initiation date | Dec 21, 2018 |
| Report date | Oct 2, 2019 |
| Termination date | Oct 27, 2020 |
| City | Andover |
| State | MA |
| Country | United States |
| FEI number | 3011391469 |
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
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: