Drug recall
Philips Multi Diagnost Eleva II with swivel cable Product Codes; 708032, 708036 Multi Diagnost Eleva with…
FDA recall event 62052 · Class II · Philips Healthcare Inc.
Key facts
| Event ID | 62052 |
|---|---|
| Recall numbers | Z-1829-2012 |
| Recalling firm | Philips Healthcare Inc. |
| Product type | Devices |
| Products | Philips Multi Diagnost Eleva II with swivel cable Product Codes; 708032, 708036 Multi Diagnost Eleva with FlatDetector with swivel cable Product Codes: 708034, 708037 This Philips MultiDiagnost Eleva… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | MultiDiagnost Eleva X--Ray system may have damage to System Cables from repeated movement |
| Initiation date | May 21, 2012 |
| Report date | Jun 27, 2012 |
| Termination date | Jan 18, 2017 |
| 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: