Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CR MD1.0 General Set Recalled by AGFA Corp. Due to The cassettes were shipped with the wrong IP...
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
CR MD1.0 General Set, x-ray imager image plate. CR 10-X Image Plate 35CM X 43CM. An image plate, contained in an X-Ray cassette, used to capture images from X-Ray exposures. The cassette with the image plate, once exposed, is inserted in the Agfa Digitizer CR 10-X where the image plate is taken out of the cassette and then scanned so that the scanned image can be displayed for viewing.
Quantity: 17
Why Was This Recalled?
The cassettes were shipped with the wrong IP (image plate) size bar code.
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