Lower riskMedical device recall · FDA · Published June 30, 2026
Merge PACS Workstation Recalls: Patient Study Thumbnails Display Issue
Merge Healthcare recalls medical imaging workstations where thumbnails from opened patient studies may display incorrectly. Affected versions include 9.4, 9.4 P01, and :9.4 P02. No immediate action needed.
“Merge PACS Workstation Recalls: Patient Study Thumbnails Display Issue.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/314296-merge-pacs-workstation-recalls-patient-study-thumbnails-display-issue. Based on FDA recall #Z-2874-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2874-2026%22&limit=1).
Merge Healthcare, Inc. voluntarily recalled Merge PACS medical imaging diagnostic workstations on June 30, 2026, according to the FDA. The hazard involves thumbnails from a previously opened patient study potentially displaying while a different study is open.
How to tell if you have it
Brand: Merge Healthcare
Product: Merge PACS, medical imaging diagnostic workstation
UPCs: 00842000101154, 00842000101215
Affected Versions: 9.4, 9.4 P01, and 9.4 P02
Units affected: 53
The hazard
Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.
Context
GovInfoNow's records show Merge Healthcare, Inc. has 11 other recalls on record since June 13, 2017. Other recent recalls of similar products include GE Healthcare Centricity PACS Software Recall (July 31, 2026), GE Healthcare Centricity PACS Server V7 Recall (July 31, 2026), and GE Healthcare Workflow Core Services V8 Recall (July 31, 2026).
How to tell if you have this one
Check if your Merge PACS workstation has software versions 9.4, 9.4 P01, or 9.4 P02. The UDI codes (01)00842000101215(10)9.4.0.P01(11)250916 and (01)00842000101154(10)9.4.0.P02(11)260302 are associated with these versions.
Brand
Merge Healthcare
Product
Merge PACS, medical imaging diagnostic workstation
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, and UK.
Recall number
Product, codes & lots
Quantity
Z-2874-2026
Merge PACS, medical imaging diagnostic workstation; UDI (01)00842000101215(10)9.4.0.P01(11)250916, (01)00842000101154(10)9.4.0.P02(11)260302 with Affected Versions: 9.4, 9.4 P01, and 9.4 P02.
53 units
Z-2875-2026
Merge OrthoPACS, medical imaging diagnostic workstation; UDI/DI (01)00842000101154(10)9.4.0.P02(11)260302, with Affected Versions: 9.4, 9.4 P01, and 9.4 P02.
5 units
Based on the official FDA remedy
What to do — step by step
Check Software Version
Verify your workstation's software version to see if it matches 9.4, 9.4 P01, or 9.4 P02.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Worldwide distribution - US Nationwide and the countries of Canada, and UK.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 43 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-2874-2026 (June 30, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2874-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.