Drug recall
Mobile Detector Holder - Stationary X-ray System (RF System). suitable for positioning the wireless portable…
FDA recall event 78833 · Class II · Philips Electronics North America Corporation
Key facts
| Event ID | 78833 |
|---|---|
| Recall numbers | Z-0311-2018 |
| Recalling firm | Philips Electronics North America Corporation |
| Product type | Devices |
| Products | Mobile Detector Holder - Stationary X-ray System (RF System). suitable for positioning the wireless portable detector free in the room for X-ray exposures. It supports the wireless portable detector… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | If the lock mechanism of the movable camp of the mobile detector holder is not adjusted properly or not secured, the portable detector can drop down when the moveable clamp is at the bottom (below of… |
| Initiation date | Jul 14, 2017 |
| Report date | Jan 10, 2018 |
| Termination date | Jun 5, 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: