Class II — Potential Health Hazard

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...

Date: June 23, 2022
Company: DICOM Grid, Inc. d/b/a Ambra Health
Status: Ongoing
Source: FDA (Device)

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

Affected (42 states)Not affected

About DICOM Grid, Inc. d/b/a Ambra Health

DICOM Grid, Inc. d/b/a Ambra Health has 1 total recall tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report