FDA Device recall Z-2072-2012
EOS X-ray Medical Diagnostic , X-ray Equipment System Digital Radiography used in general radiographic examination
- FDA Device
- Class II
- terminated
- Published 2012-10-10
On 2012-10-10 the FDA classified a Class II recall of EOS X-ray Medical Diagnostic , X-ray Equipment System Digital Radiography used in general radiographic examination by Eos Imaging, citing it was discovered of several generator failures of the EOS System due to failure of its anode controller board that drives the rotation of the X-ray tube anode.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2072-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-06-19 |
| Published | 2012-10-10 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Eos Imaging |
| Distribution | US |
Product
EOS X-ray Medical Diagnostic , X-ray Equipment System Digital Radiography used in general radiographic examination.
Reason
It was discovered of several generator failures of the EOS System due to failure of its anode controller board that drives the rotation of the X-ray tube anode.
Identifiers
| code_info | All associated Serial Numbers |
|---|
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-2072-2012%22
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