DrugApr 1, 2026
SODIUM IODIDE I-131 Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit recall — FDA D-0401-2026
Failed Tablet/Capsule Specifications
Class IIIFDA: OngoingRadnostix
Recall history in this database
Classification mix: Class III: 1, Class II: 1.
DrugMar 11, 2026
Sodium Iodide (I-131) Solution, Therapeutic Oral, packaged as a) 1 ml V-vial, NDC recall — FDA D-0389-2026
Presence of Particulate Matter: Due to production issues
Class IIFDA: OngoingRadnostix
Understanding this recall history
This page summarizes recall records in which the official source identifies Radnostix as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.