Z-1427-2017Class II

Juno DRF; Model: 709020

Name: Z-1427-2017 Juno DRF; Model: 709020
Creator: Villa Sistemi Medicali S.P.A.
Published: 2016-12-27
License: https://open.fda.gov/license/

Villa Sistemi Medicali S.p.A. / initiated 2016-12-27 / Terminated / root cause: manufacturing process

FDA source

Villa Sistemi Medicali S.P.A. began a recall of Juno DRF; Model: 709020 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures on 2016-12-27. FDA classified it as Class II and gives the reason as "Patient fell from the table because the footrest of the device detached from the table top while the patient was positioned on the table and table was moving from vertical position". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-1427-2017
Classification: Class II
Status: Terminated
Initiated: 2016-12-27
Posted: 2017-03-09
Terminated: 2021-03-09
Recalling firm: Villa Sistemi Medicali S.p.A.
Product: Juno DRF; Model: 709020 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures
Product code: KXJ Table, Radiologic
Reason for recall: Patient fell from the table because the footrest of the device detached from the table top while the patient was positioned on the table and table was moving from vertical position.
Root cause tag: manufacturing process
FDA root cause: Nonconforming Material/Component
Action: Customers were notified of the recall via DHL or similar mail service. The letter identified the affected product, problem and actions to be taken.
Quantity in commerce: 65 devices in total
Distribution: US Nationwide distribution in the states of AL, AZ, CA, CO, CT, DC, FL, IA, IL, IN, LA, MA, MD, MI, MN, MO, MS, NJ, NY, PA, Puerto Rico, TN, TX, UT, and W.I
Product codes and lots: Serial Numbers: 10110770 11030805 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 15121505 16011512 16021514 16021517 16021518 16041533 16121595

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1427-2017
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1427-2017	Class II	Terminated	Voluntary: Firm initiated	2017-03-15	2017-03-09
Z-1428-2017	Class II	Terminated	Voluntary: Firm initiated	2017-03-15	2017-03-09
Z-1429-2017	Class II	Terminated	Voluntary: Firm initiated	2017-03-15	2017-03-09
Z-1430-2017	Class II	Terminated	Voluntary: Firm initiated	2017-03-15	2017-03-09

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)