Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Juno DRF Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from the table because the footrest...
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 Sistemi Medicali S.P.A. directly.
Affected Products
Juno DRF; Model: 709020 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures
Quantity: 65 devices in total
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Villa Sistemi Medicali S.P.A.
Villa Sistemi Medicali S.P.A. 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