Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CombiDiagnost R90 1.0 (709030) Recalled by PHILIPS MEDICAL SYSTEMS Due to While performing a fluoroscopy examination, there is a...
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 MEDICAL SYSTEMS directly.
Affected Products
CombiDiagnost R90 1.0 (709030)
Quantity: 86 units
Why Was This Recalled?
While performing a fluoroscopy examination, there is a potential that the Radio Fluoroscopy (RF) viewer will also display a previous patient's radiography images. If the issue occurs, there will be differences in image content, image format and image size.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About PHILIPS MEDICAL SYSTEMS
PHILIPS MEDICAL SYSTEMS has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report