Omnipaque recalls
Omnipaque products have been recalled 3 times, most recently on 15 Apr 2026. The recalling company is usually GE Healthcare Ireland. The most common reason is particulate matter.
Total recalls3since 2018
Last 12 months2reported
Class I00% of total
Ongoing2latest 15 Apr 2026
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 omnipaque is recalled
Companies
Product types
By year
Ongoing omnipaque recalls
2 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | GE Healthcare Omnipaque (iohexol) Injection, 300 mg/mL 7%) recalledOmnipaque | GE Healthcare Ireland | Particulate Matter | Nationwide |
| Drug | CLASS II | GE Healthcare Omnipaque (iohexol) Injection, 350 mg/mL 7%) recalledOmnipaque | GE Healthcare Ireland | Particulate Matter | Nationwide |
All omnipaque recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | GE Healthcare Omnipaque (iohexol) Injection, 300 mg/mL 7%) recalledOmnipaque | GE Healthcare Ireland | Particulate Matter | Nationwide |
| Drug | CLASS II | GE Healthcare Omnipaque (iohexol) Injection, 350 mg/mL 7%) recalledOmnipaque | GE Healthcare Ireland | Particulate Matter | Nationwide |
| Drug | CLASS II | Omnipaque (iohexol) Injection, 180mgI/mL Single-Dose Vial recalledOmnipaque | GE Healthcare Inc. Life Sciences | Particulate Matter | TN |
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.