Device recall: Villa Sistemi Rotograph EVO 3D X-ray
Class II FDA enforcement event 71958. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
It has been discovered that due to lack of information accompanying documents the product fails to comply with 21CfR 1020.33(c),1020.33(d),1020.33(g),and 1020.330).
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Villa Radiology Systems LLC started this device recall on 5 Aug 2015. The firm address in the FDA record is in Oxford, CT. FDA put the recall in Class II. FDA event 71958 has 2 product records. The first FDA enforcement report date is 18 Nov 2015. The record gives the status Terminated, with the termination date 22 Mar 2017.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
US Distribution
Recalling firm
Villa Radiology Systems LLC, Oxford, CT.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
2 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-0128-2016 | Villa Sistemi Rotograph EVO 3D X-ray | Rotograph EVO 3D - 8 installed | Class II | Terminated | 18 Nov 2015 |
| Z-0129-2016 | Owandy Radiology I -MAX Touch 3D X-ray | I-MAX Touch 3D- 6 installed | Class II | Terminated | 18 Nov 2015 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Device events that started in 2015
- 1,153
- Share of these events in Class II
- 91%
- Product records in this event
- 2Median of the firm: 2
- Events of the firm on the register
- 4
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 19 Feb 2016 | Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures. | Device | Class II | 4 |
| 14 Dec 2014 | Juno DFR X-ray system | Device | Class II | 1 |
| 2 Aug 2013 | Juno DRF System. Mobile X-ray system These are general, multi-function x-ray systems capable of routine radiographs and | Device | Class II | 1 |
Official channels
- FDA enforcement report Z-0128-2016The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
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Cite this page
Recall Register. FDA enforcement event 71958. https://recallregister.com/fda/ii/71958/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA device enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
US Distribution
- What quantity of product is in FDA event 71958?
- The event has 2 product records. The first record gives this quantity:
Rotograph EVO 3D - 8 installed
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many device recalls of 2015 have the same class?
- 91% of the 1,153 device events that started in 2015 are in Class II.