Juno DFR X-ray system — Class II medical device recall Z-1079-2015
Terminated recall by Villa Radiology Systems LLC, reported 2015-03-18, distributed in AL, AZ, CA, CO, CT, DC, FL, IA…. The system does not provide the appropriate audible signal, permanent activation, and manual override, althoug
| Recall number | Z-1079-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Villa Radiology Systems LLC, Oxford, CT, United States |
| Recall initiated | 2014-12-14 |
| Classified | 2015-03-06 |
| Reported by FDA | 2015-03-18 |
| Terminated | 2017-03-16 |
| Distributed | AL, AZ, CA, CO, CT, DC, FL, IA, IL, IN, MA, MD, MI, MO, MS, NY, OH, PA, TN, TX, UT |
| Quantity | 30 units |
Product
Juno DFR X-ray system
Reason for recall
The system does not provide the appropriate audible signal, permanent activation, and manual override, although the system is in high-level control functionality
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1079-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
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.