Sodium Iodide I-131 recalls
Sodium Iodide I-131 products have been recalled 2 times, most recently on 1 Apr 2026. The recalling company is usually Radnostix. The most common reason is packaging defects.
Total recalls2since 2026
Last 12 months2reported
Class I00% of total
Ongoing2latest 1 Apr 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 50%Class III 1 50%
Why sodium iodide i-131 is recalled
Companies
Product types
By year
Ongoing sodium iodide i-131 recalls
2 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Gelatin Capsule Pack for use recalled by RadnostixSodium Iodide I-131 | Radnostix | Packaging Defects | Nationwide |
| Drug | CLASS II | Sodium Iodide (I-131) Solution, Therapeutic Oral recalled by RadnostixSodium Iodide I-131 | Radnostix | Particulate Matter | Nationwide |
All sodium iodide i-131 recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Gelatin Capsule Pack for use recalled by RadnostixSodium Iodide I-131 | Radnostix | Packaging Defects | Nationwide |
| Drug | CLASS II | Sodium Iodide (I-131) Solution, Therapeutic Oral recalled by RadnostixSodium Iodide I-131 | Radnostix | Particulate Matter | 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.