Sodium Iodide I-131 recalls

The FDA has published 3 recalls involving Sodium Iodide I-131 since 2016. The latest was reported on 1 Apr 2026. Most were for packaging defects. Radnostix has the most recalls in this group. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls3since 2016
Last 12 months2reported
Class I00% of total
Ongoing2latest 1 Apr 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 1 33%Class III 2 67%

Why sodium iodide i-131 is recalled

By year

Ongoing sodium iodide i-131 recalls

2 active
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIIGelatin Capsule Pack for use recalled by RadnostixSodium Iodide I-131RadnostixPackaging DefectsNationwide
DrugCLASS IISodium Iodide (I-131) Solution, Therapeutic Oral recalled by RadnostixSodium Iodide I-131RadnostixParticulate MatterNationwide

All sodium iodide i-131 recalls, newest first

3 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIIGelatin Capsule Pack for use recalled by RadnostixSodium Iodide I-131RadnostixPackaging DefectsNationwide
DrugCLASS IISodium Iodide (I-131) Solution, Therapeutic Oral recalled by RadnostixSodium Iodide I-131RadnostixParticulate MatterNationwide
DrugCLASS IIISodium Iodide I, USP Diagnostic Oral recalled by Jubilant DraximageSodium Iodide I 131 DiagnosticJubilant DraximageOtherNationwide

Should you stop taking Sodium Iodide I-131?

Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.