Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DEXIS Imaging Suite - catalog number 1.008.7932 Recalled by Imaging Sciences International, LLC Due to A condition can occur during renumbering of the...
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 Imaging Sciences International, LLC directly.
Affected Products
DEXIS Imaging Suite - catalog number 1.008.7932, version numbers 10.0.0 through 10.0.3 Radiological Image Processing System
Quantity: 366
Why Was This Recalled?
A condition can occur during renumbering of the patient database using the DEXCopy feature. When renumbering is being performed using the DEXCopy feature and multiple patients with an identical name are present, the software will assign all subsequent records to the first patient record, resulting in mixed patient records. In order for this problem to occur several conditions need to be met: 1)
Where Was This Sold?
This product was distributed to 42 states: AL, AZ, AR, CA, CO, CT, DE, FL, GA, IL, IN, IA, KS, KY, LA, MD, MA, MI, MN, MO, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, DC
About Imaging Sciences International, LLC
Imaging Sciences International, LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report