IMPRIS Imaging recalls
IMPRIS Imaging has 4 recalls on record with the FDA and USDA, the earliest in 2025 and the latest reported on 5 Nov 2025. 4 are still ongoing. 4 were reported in the last 12 months. The most frequent reason is packaging defects.
Total recalls4since 2025
Last 12 months4reported
Class I4100% of total
Ongoing4latest 5 Nov 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 4 100%Class II 0 0%Class III 0 0%
Why impris imaging is recalled
Product types
By year
Ongoing impris imaging recalls
4 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS I | Imris Operating Suite, iMRI 3T S recalled by IMPRIS Imaging | IMPRIS Imaging | Packaging Defects | Nationwide |
| Device | CLASS I | Imris Operating Suite, Imris iMRI 3T V recalled by IMPRIS Imaging | IMPRIS Imaging | Packaging Defects | Nationwide |
| Device | CLASS I | Imris Operating Suite, InVision 3T Operating Suite recalled | IMPRIS Imaging | Packaging Defects | Nationwide |
| Device | CLASS I | Imris Operating Suite, Neuro Iii-sv iMRI System recalled | IMPRIS Imaging | Packaging Defects | Nationwide |
All impris imaging recalls, newest first
4 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS I | Imris Operating Suite, iMRI 3T S recalled by IMPRIS Imaging | IMPRIS Imaging | Packaging Defects | Nationwide |
| Device | CLASS I | Imris Operating Suite, Imris iMRI 3T V recalled by IMPRIS Imaging | IMPRIS Imaging | Packaging Defects | Nationwide |
| Device | CLASS I | Imris Operating Suite, InVision 3T Operating Suite recalled | IMPRIS Imaging | Packaging Defects | Nationwide |
| Device | CLASS I | Imris Operating Suite, Neuro Iii-sv iMRI System recalled | IMPRIS Imaging | Packaging Defects | 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.