DICOM Grid, Inc. d/b/a Ambra Health Ambra PACS, Ambra ProViewer recall — FDA Z-1818-2022
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.
Overview of recall records associated with DICOM Grid, Inc. d/b/a Ambra Health, including dates, categories and classifications where available.
Classification mix: Class II: 1.
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.
This page summarizes recall records in which the official source identifies DICOM Grid, Inc. d/b/a Ambra Health as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.