United StatesGelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (contains 5 empty capsules and 5 Dibasic Sodium Phosphate 300 mg, International Isotopes Inc., NDC 69208-003-15, 69208-003-25, 69208-003-35; Lots 3666245 exp 02/28/2026, 4546213 exp 02/28/2026, 4951280 exp 09/30/2027) is being recalled by Radnostix. The recall is due to failed tablet/capsule specifications and is ongoing; affected units were distributed nationwide in the United States, including Puerto Rico.
What's being 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
Recalling firm: Radnostix, Idaho Falls, ID, United States.
How to identify it
Lot, expiry: Lot 3666245, exp: 02/28/2026; Lot 4546213, exp: 02/28/2026 and Lot 4951280, exp 09/30/2027
The hazard
Failed Tablet/Capsule Specifications
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
Nationwide in the US, including Puerto Rico
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)