Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Villa Radiology Systems with 8 device recalls. The most recent is a device recall dated Feb 19, 2016: Apollo: Models: 9784000131, 9784000231, 9784020131, 9784020231, 9784100231, 9784120131, ….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Feb 19, 2016 | Apollo: Models: 9784000131, 9784000231, 9784020131, 9784020231, 9784100231, 9784120131, 9784120231, 9784130131 Multi-function x-ray systeClass II · The analysis showed that the incident was caused by a chain of four faults: 1.) The injured person overcame a physical | Device recalls |
| Feb 19, 2016 | Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.Class II · The analysis showed that the incident was caused by a chain of four faults: 1.) The injured person overcame a physical | Device recalls |
| Feb 19, 2016 | Apollo DRF: Model: 9784220831 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.Class II · The analysis showed that the incident was caused by a chain of four faults: 1.) The injured person overcame a physical | Device recalls |
| Feb 19, 2016 | Apollo EZ: Model: 9784152036 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.Class II · The analysis showed that the incident was caused by a chain of four faults: 1.) The injured person overcame a physical | Device recalls |
| Aug 5, 2015 | Owandy Radiology I -MAX Touch 3D X-rayClass II · It has been discovered that due to lack of information accompanying documents the product fails to comply with 21CfR 102 | Device recalls |
| Aug 5, 2015 | Villa Sistemi Rotograph EVO 3D X-rayClass II · It has been discovered that due to lack of information accompanying documents the product fails to comply with 21CfR 102 | Device recalls |
| Dec 14, 2014 | Juno DFR X-ray systemClass II · The system does not provide the appropriate audible signal, permanent activation, and manual override, although the syst | Device recalls |
| Aug 2, 2013 | Juno DRF System. Mobile X-ray system These are general, multi-function x-ray systems capable of routine radiographs and general fluoroscoClass II · It has been discovered that the Air Kerma rate information is inconsistent in Continuous Fluoro modes 30x30 (12"x12") an | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
