Radnostix recalls Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (containing 5 empty capsules and 5 Dibasic Sodium Phosphat
Recalled April 1, 2026 · FDA recall D-0401-2026 · Radnostix
Hazard
Failed Tablet/Capsule Specifications · FDA Class III
Units
2,699 blister cartons
Sold at
Nationwide in the US, including Puerto Rico
Description
Failed Tablet/Capsule Specifications
Product
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
Manufacturer(s)
Radnostix
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →