Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DX-D 600 DIRECT RADIOGRAPHY SYSTEM Product Usage: The DX-D 600 Recalled by Agfa-Gevaert, N.V. Due to After an upgrade of the software of the...
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 Agfa-Gevaert, N.V. directly.
Affected Products
DX-D 600 DIRECT RADIOGRAPHY SYSTEM Product Usage: The DX-D 600 system is a ceiling mounted General Radiography X-Ray imaging system used in hospitals, clinics and medical practices by physicists, radiographers and radiologists to make, process and view static X-Ray radiographic images of the skeleton (including skull, spinal column and extremities), chest, abdomen and other body parts on adult, pediatric or neonatal patients.
Quantity: 10
Why Was This Recalled?
After an upgrade of the software of the Overhead Tube Crane, there were isolated cases in which the Overhead Tube Crane movement does not stop when the movement button is released. Instead of stopping while the movement button is released, the Tube Head Crane moves to the intended position.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Agfa-Gevaert, N.V.
Agfa-Gevaert, N.V. 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