Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
KODAK DirectView DR 9000 System Recalled by Carestream Health Inc. Due to A control system failure may cause the U-Arm...
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 Carestream Health Inc. directly.
Affected Products
KODAK DirectView DR 9000 System, Catalog Numbers 1966688 (US and Canada) and 8161937 (outside the US and Canada) --- A permanently installed diagnostic x-ray system composed of 3 main components: an operator console, U-Arm assembly with x-ray tube including a collimator, and a stationary generator.
Quantity: Domestic: 100 units; Foreign: 46 units
Why Was This Recalled?
A control system failure may cause the U-Arm to move downward unexpectedly when the Radiology Technologist is positioning the equipment using the "Up" or "Down" control buttons. Downward movement occurs at three times the normal rate of speed and will continue until the device control button is released, the Emergency Stop button is activated or the equipment Bump Sensor contacts an object.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Carestream Health Inc.
Carestream Health Inc. has 61 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report