Intelerad Medical Systems recalls
Intelerad Medical Systems has 3 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 3 Dec 2025. 2 are still ongoing. 1 was reported in the last 12 months. The most frequent reason is device malfunction.
Total recalls3since 2014
Last 12 months1reported
Class I00% of total
Ongoing2latest 3 Dec 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 3 100%Class III 0 0%
Why intelerad medical systems is recalled
Product types
By year
Ongoing intelerad medical systems recalls
2 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | IntelePACS - InteleConnect / TechPortal recalled | Intelerad Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | IntelePACS (Image Fusion Module) - InteleViewer recalled | Intelerad Medical Systems | Device Malfunction | Nationwide |
All intelerad medical systems recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | IntelePACS - InteleConnect / TechPortal recalled | Intelerad Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | IntelePACS (Image Fusion Module) - InteleViewer recalled | Intelerad Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | IntelePACS software versions 3-8-1 to 4-9-1, Product Usage recalled | Intelerad Medical Systems | Device Malfunction | Nationwide |
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.