Radnostix recalls Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (containing 5 empty capsules and 5 Dibasic Sodium Phospha…

Recall date

February 19, 2026

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0401-2026

FDA classification

Class III

Brand / firm

Radnostix

Sold / distributed

Nationwide in the US, including Puerto Rico

Why it was recalled

Failed Tablet/Capsule Specifications

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (containing 5 empty capsules and 5 Dibasic Sodium Phosphate Capsules 300 mg, International Isotopes Inc., Idaho Falls, ID 83401. NDC: 69208-003-15; 69208-003-25; 69208-003-35