Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bucky Stand SU-4000 Input 2017.11.17. SU41711085 Date: 2017-11-17 Recalled by Konica Minolta Healthcare, Americas, Inc. Due to Unintentional U-Arm movement
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 Konica Minolta Healthcare, Americas, Inc. directly.
Affected Products
Bucky Stand SU-4000 Input 2017.11.17. SU41711085 Date: 2017-11-17; Board Name; Board Version, Firmware Version Advanced Universal U-Arm 4000 System. The Positioner consists of the following associated subassemblies: Vertical Column, Swivel Arm with variable height, X-ray Tube, Automatic Exposure Control, Collimator, Touch Screen Control and Image Receptor Assembly. The Positioner and the Patient Mobile Table are associated equipment to the Generator X-ray Unit.
Quantity: 151
Why Was This Recalled?
Unintentional U-Arm movement
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Konica Minolta Healthcare, Americas, Inc.
Konica Minolta Healthcare, Americas, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report