EOS X-ray Medical Diagnostic — Class II medical device recall Z-2072-2012
Terminated recall by Eos Imaging Inc, reported 2012-10-10, distributed nationwide. It was discovered of several generator failures of the EOS System due to failure of its anode controller board
| Recall number | Z-2072-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Eos Imaging Inc, Cambridge, MA, United States |
| Recall initiated | 2012-06-19 |
| Classified | 2012-09-28 |
| Reported by FDA | 2012-10-10 |
| Terminated | 2013-09-16 |
| Distributed | Nationwide (US) |
| Quantity | 12 eos |
Product
EOS X-ray Medical Diagnostic , X-ray Equipment System Digital Radiography used in general radiographic examination.
Reason for recall
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.
Machine access
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Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.