Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stationary Fluoroscopic X-ray System CombiDiagnost R90 Recalled by Philips Medical Systems Gmbh, DMC Due to kV/mA lockin not functioning as specified which may...
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 Gmbh, DMC directly.
Affected Products
Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationary Fluoroscopic X-ray System
Quantity: 146
Why Was This Recalled?
kV/mA lockin not functioning as specified which may result in the patient receiving an increased radiation dose.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Medical Systems Gmbh, DMC
Philips Medical Systems Gmbh, DMC has 33 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report