Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Model Kodak 2200 Intraoral X-Ray System Recalled by Carestream Health Inc. Due to Carestream received problem reports relating to apparent early...
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
Model Kodak 2200 Intraoral X-Ray System, Catalog Numbers 5303177, 5303169, 5303151, XR-5154323 -- Carestream Health, Inc. Made in France -- --- COMMON/USUAL NAME: Dental X-Ray Systems -- CLASSIFICATION NAME: Unit, X-Ray, Extraoral with timer --- There are four major components: x-ray tube, x-ray generator, collimator and image receptor. These systems are permanently installed diagnostic dental x-ray systems for generation of x-rays for examination of the teeth, jaw and oral structures.
Quantity: Domestic: 347 units (total for both)
Why Was This Recalled?
Carestream received problem reports relating to apparent early failure of Kodak 2X00 Intraoral X-ray device arms leading to arm breakage.
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