FDA Device recall Z-0431-2014
Easy Diagnost Eleva Universal Fluoroscopic applications
- FDA Device
- Class II
- terminated
- Published 2013-12-11
On 2013-12-11 the FDA classified a Class II recall of Easy Diagnost Eleva Universal Fluoroscopic applications by Philips Medical Systems, citing the delivered application software was an outdated version to the model of equipment.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0431-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-10-30 |
| Published | 2013-12-11 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Philips Medical Systems |
| Distribution | US |
Product
Easy Diagnost Eleva Universal Fluoroscopic applications
Reason
The delivered application software was an outdated version to the model of equipment.
Identifiers
| code_info | 706050, 706083, 706088 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0431-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.