Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Agfa Digital Radiography X-Ray System DX-D 100 Product Usage: Is Recalled by AGFA Healthcare Corp. Due to Mislabeling
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 Digital Radiography X-Ray System DX-D 100 Product Usage: Is indicated for use in providing diagnostic quality images to aid the physician with diagnoses.
Quantity: 1
Why Was This Recalled?
Unit was mislabeled with a factory label showing 32 KW output power.
Where Was This Sold?
This product was distributed to 1 state: WV
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