Villa Radiology Systems LLC recalls

7 recalls on record · latest: February 19, 2016

Official U.S. recall history for Villa Radiology Systems LLC, compiled from official government records.

Get recall alerts

Free email alert whenever Villa Radiology Systems LLC has a new recall — straight from official government data. Unsubscribe anytime.

Villa Radiology Systems LLC recalls Apollo: Models: 9784000131, 9784000231, 9784020131, 9784020231, 9784100231, 9784120131, 9784120231, 9784130131 Multi-fu…

February 19, 2016 · Medical device recalls Moderate risk The analysis showed that the incident was caused by a chain of four faults: 1.)…

Villa Radiology Systems LLC recalls Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.

February 19, 2016 · Medical device recalls Moderate risk The analysis showed that the incident was caused by a chain of four faults: 1.)…

Villa Radiology Systems LLC recalls Apollo DRF: Model: 9784220831 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy proced…

February 19, 2016 · Medical device recalls Moderate risk The analysis showed that the incident was caused by a chain of four faults: 1.)…

Villa Radiology Systems LLC recalls Apollo EZ: Model: 9784152036 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedu…

February 19, 2016 · Medical device recalls Moderate risk The analysis showed that the incident was caused by a chain of four faults: 1.)…

Villa Radiology Systems LLC recalls Owandy Radiology I -MAX Touch 3D X-ray

August 5, 2015 · Medical device recalls Moderate risk It has been discovered that due to lack of information accompanying documents t…

Villa Radiology Systems LLC recalls Villa Sistemi Rotograph EVO 3D X-ray

August 5, 2015 · Medical device recalls Moderate risk It has been discovered that due to lack of information accompanying documents t…

Villa Radiology Systems LLC recalls Juno DFR X-ray system

December 14, 2014 · Medical device recalls Moderate risk The system does not provide the appropriate audible signal, permanent activatio…