Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
KODAK DirectView DR 7500 Dual Detector System Recalled by Carestream Health, Inc. Due to Carestream Health, Inc. has recalled DR 7500 Dual...
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 7500 Dual Detector System, MODEL DR 7500, Manufactured by Carestream Health, Inc. Made in U.S.A.
Quantity: 164 units Total (42 domestically & 122 internationally)
Why Was This Recalled?
Carestream Health, Inc. has recalled DR 7500 Dual Detector System utilizing Version 5.X Software due to a possible patient image display error.
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