Z-1063-2017Class II

Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy...

Name: Z-1063-2017 Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy...
Creator: Villa Radiology Systems LLC
Published: 2016-02-19
License: https://open.fda.gov/license/

Acteon, Inc. / initiated 2016-02-19 / Open, Classified / root cause: design

FDA source

Villa Radiology Systems LLC began a recall of Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures on 2016-02-19. FDA classified it as Class II and gives the reason as "The analysis showed that the incident was caused by a chain of four faults: 1.) The injured person overcame a physical barrier (the tabletop support arm. height ca. 60 em) to access a prohibited area not intended as a...". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as design.

Recall record

Recall number: Z-1063-2017
Classification: Class II
Status: Open, Classified
Initiated: 2016-02-19
Posted: 2017-01-20
Recalling firm: Acteon, Inc.
Product: Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
Product code: KXJ Table, Radiologic
Reason for recall: The analysis showed that the incident was caused by a chain of four faults: 1.) The injured person overcame a physical barrier (the tabletop support arm. height ca. 60 em) to access a prohibited area not intended as a working position. 2) The directions for use (device labeling and instructions for use) did not contain an explicit exclusion of the prohibited area. 3.) The movement was activated inadvertently and continuously. and it was not released (the movement requires continuous activation). 4.) Delayed activation of the emergency stop.
Root cause tag: design
FDA root cause: Device Design
Action: Consignees were notified of the recall via letter starting on 2/19/16. The letter explains the issue and actions to be taken by the consignee and manufacturer.
Quantity in commerce: 66 distributed in US
Distribution: AL AZ CA CO CT DC FL IA IL IN LA MA MD MI MN MO MS NJ NY OH PA Puerto Rico TN TX UT WI
Product codes and lots: 10110770 11030805 11030806 11070845 11070848 11070849 11090864 11110900 12020978 12020982 12030999 12041003 12061014 12061018 12061020 12081040 12091074 12101104 12121186 12121187 13031215 13101263 14021301 14031313 14041321 14051332 14071353 14081359 14091368 14091371 14121400 14121403 15021426 15031440 15041444 15091473 15091478 15101484 15101487

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1063-2017
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1063-2017	Class II	Ongoing	Voluntary: Firm initiated	2017-02-01	2017-01-20
Z-1064-2017	Class II	Ongoing	Voluntary: Firm initiated	2017-02-01	2017-01-20
Z-1065-2017	Class II	Ongoing	Voluntary: Firm initiated	2017-02-01	2017-01-20
Z-1066-2017	Class II	Ongoing	Voluntary: Firm initiated	2017-02-01	2017-01-20

Product code KXJ

K050190Class IIApolloVilla Sistemi Medicali S.P.A. / cleared 2005-03-25

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)