Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
OnSight 3D Extremity System- X-Ray Recalled by Carestream Health, Inc. Due to When the user performs the re-assignment of a...
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
OnSight 3D Extremity System- X-Ray, Tomography Computed System Catalog Numbers: 1743566 (w/ Attached Console) 1743574 (w/ Remote Console) The device is intended to be used for x-ray computed tomography and projection x-ray imaging of upper and lower extremities of adult patients and pediatric patients aged 12 and over.
Quantity: 37 units
Why Was This Recalled?
When the user performs the re-assignment of a parent / companion pair, the parent volume is transferred to the new patient but the companion volume will remain in the original patient s exam.
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