Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AGFA DX-D 100 is a mobile digital radiography x-ray system Recalled by AGFA Healthcare Corp. Due to When using the DX-D 100 unit, sporadic unintended...
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
AGFA DX-D 100 is a mobile digital radiography x-ray system
Quantity: 233 units
Why Was This Recalled?
When using the DX-D 100 unit, sporadic unintended movements caused by an electrostatic discharge of the unit to the ground may occur.
Where Was This Sold?
This product was distributed to 29 states: AL, CA, FL, GA, IL, IA, KY, LA, MD, MA, MI, MN, MS, MO, NE, NJ, NY, NC, OH, OK, OR, SC, TN, TX, VA, WV, WI, WY, 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