FDA Device recall Z-1829-2012
Philips Multi Diagnost Eleva II with swivel cable Product Codes
- FDA Device
- Class II
- terminated
- Published 2012-06-27
On 2012-06-27 the FDA classified a Class II recall of Philips Multi Diagnost Eleva II with swivel cable Product Codes by Philips Healthcare, citing multiDiagnost Eleva X--Ray system may have damage to System Cables from repeated movement.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1829-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-05-21 |
| Published | 2012-06-27 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Philips Healthcare |
| Distribution | US |
Product
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 system is intended to be used as a multifunctional/ universal system. General R/F, performed along with more specialized interventional applications. This includes the following general areas: Digestive system Skeletal system Urinary system Reproductive system Respiratory system Circulatory system Various . Arthrograms . Myelograms . Facet joint injections . Discography SialographyFluoroscopy, Radiography and Angiography
Reason
MultiDiagnost Eleva X--Ray system may have damage to System Cables from repeated movement
Identifiers
| code_info | Units with cable swivel delivered from 2007 |
|---|
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-1829-2012%22
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