DICOM Grid recalls

DICOM Grid has 3 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 24 Dec 2025. 2 are still ongoing. 1 was reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls3since 2017

Last 12 months1reported

Class I00% of total

Ongoing2latest 24 Dec 2025

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 1 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 3 100%Class III 0 0%

Why dicom grid is recalled

Device Malfunction267%
Labeling Errors133%

Product types

Test Kits & Diagnostics267%
Medical Software133%

By year

2025133%
2022133%
2017133%

Ongoing dicom grid recalls

2 active

Reported	Class	Recall	Company	Reason	Where
24 Dec 2025Device	CLASS II	Intelerad InteleShare recalled by DICOM Grid	DICOM Grid	Labeling Errors	44 states
5 Oct 2022Device	CLASS II	Ambra PACS, Ambra ProViewer recalled by DICOM Grid	DICOM Grid	Device Malfunction	43 states

All dicom grid recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
24 Dec 2025Device	CLASS II	Intelerad InteleShare recalled by DICOM Grid	DICOM Grid	Labeling Errors	44 states
5 Oct 2022Device	CLASS II	Ambra PACS, Ambra ProViewer recalled by DICOM Grid	DICOM Grid	Device Malfunction	43 states
25 Jan 2017Device	CLASS II	Ambra PACS recalled by Dicom Grid	Dicom Grid	Device Malfunction	27 states

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.