Drug recall
digital x-ray detector ProGrade R1 - solid state X ray imager (flat panel/digital imager) As a part of a…
FDA recall event 79139 · Class II · Philips Electronics North America Corporation
Key facts
| Event ID | 79139 |
|---|---|
| Recall numbers | Z-0704-2018 |
| Recalling firm | Philips Electronics North America Corporation |
| Product type | Devices |
| Products | digital x-ray detector ProGrade R1 - solid state X ray imager (flat panel/digital imager) As a part of a radiographic system, the Philips ProGrade is intended to acquire, process, store, display, and… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | It the WiFi connection between the SkyPlate detector and HP transfer point is weak, an image may fail to transfer from the SkyPlate detector to the system. The image remains in the memory of the… |
| Initiation date | Dec 11, 2017 |
| Report date | Mar 7, 2018 |
| Termination date | May 29, 2020 |
| City | Andover |
| State | MA |
| Country | United States |
| FEI number | 1218950 |
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: