IntelePACS Medical System Recall: Image Display Mismatch Risk
IntelePACS Medical System versions PACS-5-1-1-R102 through PACS-5-9-1-R8 have a potential image display mismatch issue. Affected units may show incorrect images when using Chromium-based web browsers. Contact InteleRad Medical Systems for details.
Lower-risk recall
Following a Chromium-based web-browser, report and displayed images may not match.
What happened, in plain English
IntelePACS medical imaging systems with specific software versions may display mismatched images when used with Chromium web browsers. This could lead to incorrect medical images being shown to healthcare providers. Read more at govinfonow.com/recall/1764695-intelerad-medical-systems-incorporated-recalls-intelepacs-inteleconnect-portal-tech-portal.
Source Summary by GovInfoNow · govinfonow.com/recall/1764695-intelerad-medical-systems-incorporated-recalls-intelepacs-inteleconnect-portal-tech-portal · Published October 27, 2026 · Updated October 27, 2026 · FDA enforcement record: FDA #Z-0186-2027
Cite this page
“IntelePACS Medical System Recall: Image Display Mismatch Risk.” GovInfoNow, updated October 27, 2026. https://govinfonow.com/recall/1764695-intelerad-medical-systems-incorporated-recalls-intelepacs-inteleconnect-portal-tech-portal. Based on FDA recall #Z-0186-2027 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0186-2027%22&limit=1).
Why it’s dangerous
The system may display images that do not match the actual content when used with Chromium-based web browsers. This could lead to incorrect medical images being shown to healthcare providers during diagnosis or treatment.
Who’s affected
Healthcare providers using IntelePACS medical imaging systems with the affected software versions are most at risk. The issue affects 317 units distributed nationwide.
How to tell if you have this one
Check for the specific software versions listed in the recall: PACS-5-1-1-R102 through PACS-5-9-1-R8. The system may have an HIBC number starting with +B228INTELEPACS0.
- Brand
IntelePACS- Category
Medical device
What to do — step by step
Check Software Version
Identify your system's software version by checking the HIBC number or the specific version codes listed in the recall.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 46 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
Questions people ask
Which IntelePACS versions are affected?
IntelePACS versions PACS-5-1-1-R102 through PACS-5-9-1-R8 are affected, including specific model numbers like PACS-5-3-1-R83 through R128.
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Where this comes from
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-0186-2027 (September 5, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0186-2027 to see it in context.
- Plain-language summary written by qwen3:4b on October 27, 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.