Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AGFA Digital Radiography X-Ray System DX-D 100 Agfa's DX-D 100 Recalled by AGFA Corp. Due to Customers could potentially experience intermittent, unintended and illogical...
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 Corp. directly.
Affected Products
AGFA Digital Radiography X-Ray System DX-D 100 Agfa's DX-D 100 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: chest, abdomen, and other body parts.
Quantity: 104
Why Was This Recalled?
Customers could potentially experience intermittent, unintended and illogical movement when using the product.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About AGFA Corp.
AGFA Corp. has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report