Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
FDR Visionary Suite Recalled by FUJIFILM Healthcare Americas Corporation Due to It was found that the shaft for mounting...
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 FUJIFILM Healthcare Americas Corporation directly.
Affected Products
FDR Visionary Suite, CH-200 Model/Version Numbers: (1) 566-16130-23, (2) 566-16130-31, (3) 566-16130-33
Quantity: 16 units
Why Was This Recalled?
It was found that the shaft for mounting the X-ray tube unit on the support may break. In addition, it was found that the protective parts might not work effectively only when the shaft was broken while being operated toward the front while lifting.
Where Was This Sold?
This product was distributed to 8 states: AK, CA, FL, IL, MA, NH, OH, WI
About FUJIFILM Healthcare Americas Corporation
FUJIFILM Healthcare Americas Corporation has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report