Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DX-D 600 - DXD Imaging Package Product Usage:Is indicated for Recalled by AGFA Healthcare Corp. Due to Some customers reported that while using the DX-D600...
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 Healthcare Corp. directly.
Affected Products
DX-D 600 - DXD Imaging Package Product Usage:Is indicated for use in providing diagnostic quality images to aid the physician with diagnosis. Systems can be used with MUSICA2 image processing to create radiographic images of the skeleton including skull, spinal column and extremities, check abdomen and other both parts.
Quantity: 17 units
Why Was This Recalled?
Some customers reported that while using the DX-D600 in room or exam preparation, the Overhead Tube Crane (OTC) showed increased velocity and uncontrolled longitudinal movement.
Where Was This Sold?
This product was distributed to 9 states: GA, IN, KS, KY, MA, NJ, SC, VA, DC
About AGFA Healthcare Corp.
AGFA Healthcare Corp. has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report