Drug recall
Philips Essenta DR, X-Ray System, Diagnostic, general-purpose Model: 712070. The Essenta DR is a…
FDA recall event 62650 · Class II · Philips Healthcare Inc.
Key facts
| Event ID | 62650 |
|---|---|
| Recall numbers | Z-2207-2012 |
| Recalling firm | Philips Healthcare Inc. |
| Product type | Devices |
| Products | Philips Essenta DR, X-Ray System, Diagnostic, general-purpose Model: 712070. The Essenta DR is a multifunctional stationary X-ray Intended Use From Labeling): system, in which the swivel arm rotation… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Essenta DR C-Arm may fall |
| Initiation date | Jul 25, 2012 |
| Report date | Aug 22, 2012 |
| Termination date | Mar 1, 2013 |
| 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: