Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DX-D600 - DXD Imaging Package Recalled by AGFA Healthcare Corp. Due to One of the dent markers from 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-D600 - DXD Imaging Package
Quantity: 81 units
Why Was This Recalled?
One of the dent markers from the DX-D600 dropped down from the overhead rail.
Where Was This Sold?
This product was distributed to 24 states: AL, CA, FL, GA, HI, IL, IN, KS, LA, MA, MN, MO, NV, NJ, NM, NY, OH, OK, OR, SC, TN, TX, 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