Ambra Health recalls software versions 3.22.2.0 and 3:22.3.0 due to potential patient information edits reverting after study ingestion. Affected users should contact support for updates.
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.
Ambra Health recalls two software versions for diagnostic imaging tools because patient information edits might revert after a study is processed. This could lead to incorrect medical records if not fixed.
The software has a race condition where patient information edits might revert after a study is processed. This could cause incorrect medical records if the issue occurs during normal use.
Healthcare providers using Ambra PACS or Ambra ProViewer software versions 3.22.2.0 and 3.22.3.0 for diagnostic imaging are most at risk. Patients are not directly affected.
Check for software versions 3.22.2.0 or 3.22.3.0 in Ambra PACS or Ambra ProViewer. The product was sold as a diagnostic imaging tool by Ambra Health.
Identify your software version by checking the product documentation or settings.
Reach out to Ambra Health support for guidance on updating to a safe version.
No, patients are not directly affected by this recall. Healthcare providers using the software are most at risk.
The recall record does not specify update instructions. Contact Ambra Health support for assistance.
Software versions 3.22.2.0 and 3.22.3.0 of Ambra PACS and Ambra ProViewer.
We’ve drafted a message you can send Ambra Health to request your refund or repair — edit it as you like.
Subject: Recall Z-1818-2022 — Ambra Health Ambra Health Hello, I own a Ambra Health that is covered by recall Z-1818-2022 from Ambra Health. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.