Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Juno DRF Recalled by Villa Radiology Systems LLC Due to The analysis showed that the incident was caused...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Villa Radiology Systems LLC directly.
Affected Products
Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
Quantity: 66 distributed in US
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 25 states: AL, AZ, CA, CO, CT, FL, IL, IN, IA, LA, MD, MA, MI, MN, MS, MO, NJ, NY, OH, PA, TN, TX, UT, WI, DC
About Villa Radiology Systems LLC
Villa Radiology Systems LLC has 8 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report