Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Juno DRF Recalled by Philips Healthcare Inc. Due to Values of fluoroscopy time, Air Kerma Rate and...
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 Philips Healthcare Inc. directly.
Affected Products
Juno DRF , X-ray system, diagnostic, Fluoroscopic, general-purpose Model: 70920 Product Usage: Universal R/F, general use
Quantity: 16 units
Why Was This Recalled?
Values of fluoroscopy time, Air Kerma Rate and Cumulated Air Kerma may not be displayed "at the fluoroscopist's working position" as per 21 CFR 1003.21
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Healthcare Inc.
Philips Healthcare Inc. has 36 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report