Devices

Device Recall Juno

Model / Serial
Serial Numbers: 10110770 11030805 11070848 11070845 11070849 11030806 11090864 11110900 12020982 114087 12030999 12061020 12041003 12061014 12061018 12081040 :
Device Class
Not Classified
Implanted device?
No
Distribution
US Nationwide Distribution including the states of AL, CA, CO, CT, IL, MD, MI, MO, NY, OH, PA
Product Description
Juno DRF , X-ray system, diagnostic, Fluoroscopic, general-purpose || Model: 70920 || Product Usage: || Universal R/F, general use
Manufacturer
Philips Healthcare Inc.
1 Event
- Recall of Device Recall Juno

Manufacturer

Philips Healthcare Inc.

Manufacturer Address
Philips Healthcare Inc., 3000 Minuteman Road, Andover MA 01810
Manufacturer Parent Company (2017)
Philips
Source
USFDA

2 devices with a similar name

Learn more about the data here

Device Recall Juno DFR Xray system

Model / Serial
P/N 709020
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
US Distribution to the states of: AZ, AL, CA, CO, CT, DC, FL, IA, IL, IN, MI, MD, MS, MA, MO, NY, OH, PA, UT, TN and TX.
Product Description
Juno DFR X-ray system
Manufacturer
Villa Radiology Systems LLC

Device Recall Juno DRF

Model / Serial
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
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
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 Description
Juno DRF; Model: 709020 || Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
Manufacturer
Villa Radiology Systems LLC

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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