Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DRX-Evolution with FF WS These products are permanently installed diagnostic Recalled by Carestream Health, Inc. Due to Carestream Health Inc. has issued a recall for...
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
DRX-Evolution with FF WS These products are permanently installed diagnostic x-ray systems composed of 4 main components: an operator console, over head tube crane, x-ray tube assembly including a collimator and stationary generator. In addition the device can use an x-ray table and /or wallstand/bucky to complete x-ray exposures. The DRX-Evolution system is a permanently installed diagnostic x-ray system for generation of x-rays for examination of various anatomical regions.
Quantity: 675 units Total (145 units domestically & 530 units internationally)
Why Was This Recalled?
Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution (FF WS and CSJ WS) and the Kodak DirectView DR 7500 System due to the potential for unexpected device movement.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Carestream Health, Inc.
Carestream Health, Inc. has 17 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report