Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ambra PACS Recalled by DICOM Grid, Inc. d/b/a Ambra Health Due to A race condition between the storage system and...
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 DICOM Grid, Inc. d/b/a Ambra Health directly.
Affected Products
Ambra PACS, Ambra ProViewer. Software for use as a primary diagnostic and analysis tool for diagnostic images.
Quantity: 671 downloads
Why Was This Recalled?
A race condition between the storage system and services database has the potential to revert edits made to patient information upon first ingestion of a study.
Where Was This Sold?
This product was distributed to 42 states: AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, MD, MA, MI, MN, MS, MO, NE, NV, NH, NJ, NM, NY, NC, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WV, WI, DC
About DICOM Grid, Inc. d/b/a Ambra Health
DICOM Grid, Inc. d/b/a Ambra Health 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