Recall Register

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Villa Radiology Systems LLC

FDA recalling firm · 4 enforcement events · 8 product records · 2013–2016 · CT

Villa Radiology Systems LLC has 4 FDA enforcement events on this register (8 product records) between 2013 and 2016: 4 device; the busiest year was 2013 with 1.

0% of its events are Class I; the most common class is Class II (4). 1 event is listed as ongoing; the recalling firm's address is in CT.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
19 Feb 2016Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.DeviceClass II4Ongoing
5 Aug 2015Villa Sistemi Rotograph EVO 3D X-rayDeviceClass II2Terminated
14 Dec 2014Juno DFR X-ray systemDeviceClass II1Terminated
2 Aug 2013Juno DRF System. Mobile X-ray system These are general, multi-function x-ray systems capable of routine radiographs and general fluoroscopy proceduresDeviceClass II1Terminated

By type and class

Device4
Class II4

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

13
15
17
19
21
23
25
Enforcement events for Villa Radiology Systems LLC by year initiated.

Questions and answers

How many FDA recalls has Villa Radiology Systems LLC had?

4 enforcement events (8 product records) on this register, 2013–2016: 4 device.

Are any Villa Radiology Systems LLC recalls ongoing?

1 event is listed as ongoing in the current openFDA export.

What class are Villa Radiology Systems LLC recalls?

4 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.